| Symbol | SOLV |
|---|---|
| Name | SOLVENTUM CORP |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Surgical & Medical Instruments & Apparatus |
| Address | C/O 3M COMPANY, ST. PAUL, MN 55144-1000 |
| Telephone | 651-733-1110 |
| Fax | — |
| — | |
| Website | https://www.solventum.com/en-us/home |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001964738 |
| Description | Solventum originates from two words: solving and momentum.Solving captures the companys dedication to finding breakthrough solutions. The organization will listen closely to health care professionals and never stop solving for them -and the many lives they enhance globally. Momentum symbolizes swifter, nimbler innovation. As the independent health care company builds on every achievement, large and small, its momentum propels it past barriers, towards breakthroughs. The new name represents how the independent health care company will focus on solving big health care challenges and emphasizes the tremendous impact it can make on the world. Additional info from NASDAQ: |
Solventum to Report Second Quarter Fiscal 2026 Earnings on August 5, 2026
Read moreNew Form SD - Solventum Corp <b>Filed:</b> 2026-05-29 <b>AccNo:</b> 0001964738-26-000033 <b>Size:</b> 73 KB
Read moreDirector COX CARRIE SMITH 🟢 acquired 4.8K shares (1 derivative) of Solventum Corp (SOLV) Transaction Date: May 15, 2026 | Filing ID: 000006
Read moreDirector DeVore Susan D. 🟢 acquired 3.3K shares (1 derivative) of Solventum Corp (SOLV) Transaction Date: May 15, 2026 | Filing ID: 000008
Read moreDirector Edwards Shirley Ann 🟢 acquired 3.3K shares (1 derivative) of Solventum Corp (SOLV) Transaction Date: May 15, 2026 | Filing ID: 000009
Read moreDirector EISENBERG GLENN A 🟢 acquired 3.3K shares (1 derivative) of Solventum Corp (SOLV) Transaction Date: May 15, 2026 | Filing ID: 000012
Read moreDirector Harris Bernard A Jr 🟢 acquired 3.3K shares (1 derivative) of Solventum Corp (SOLV) Transaction Date: May 15, 2026 | Filing ID: 000006
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT07356323 | A Prospective, Single-arm, Trial to Determine Contamination Rates When Using an… | Na | Arthroplasty Replacement, Knee | Recruiting | 2026-02-19 | 2026-10-01 | ClinicalTrials.gov |
| NCT07261137 | Efficacy of Solventum™ Vitrebond™ Pulp Protect Liner/Base Used as a Liner/Base … | Na | Caries, Dental | Not_Yet_Recruiting | 2026-01-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07231237 | Clinical Study Evaluating Solventum™ Vitrebond™ Pulp Protect Liner/Base for Dir… | Na | Dental Caries | Not_Yet_Recruiting | 2026-01-01 | 2032-02-01 | ClinicalTrials.gov |
| NCT06625385 | A Study Evaluating the Safety and Efficacy of the 3M™ V.A.C. Peel and Place Dre… | Na | Wound | Recruiting | 2025-01-20 | 2027-05-01 | ClinicalTrials.gov |
| NCT05748392 | 3M Veraflo™ Cleanse Choice Complete™ (VFCCC) Clinical Study | Na | WOUNDS INJURIES | Withdrawn | 2023-06-01 | 2023-06-01 | ClinicalTrials.gov |
| NCT05361746 | Scotchbond Universal Plus Compared to Scotchbond Universal With Filtek Universa… | Na | Class V Non-carious Cervical Dental Lesions | Completed | 2022-08-18 | 2025-09-11 | ClinicalTrials.gov |
| NCT04712019 | Evaluating Edema and Range of Motion Using Negative Pressure Therapy vs. Standa… | Na | Surgical Wound | Terminated | 2020-11-06 | 2022-08-26 | ClinicalTrials.gov |
| NCT04279574 | Clinical Performance of Chairside CAD/CAM Restorations | Na | Dental Cements | Completed | 2020-08-26 | 2024-05-22 | ClinicalTrials.gov |
| NCT04756154 | Efficacy Study of Patient Preoperative Preps In-vivo | Phase3 | Surgical Skin Preparation | Completed | 2020-07-06 | 2021-04-28 | ClinicalTrials.gov |
| NCT04601103 | 3M Oral Rinse Incidence and Patient Acceptance of Sloughing When Used With Sodi… | Na | Oral Mucosal Disorder | Terminated | 2020-01-06 | 2020-03-10 | ClinicalTrials.gov |
| NCT04186806 | Evaluation of the Efficacy of 3M Dry Mouth Moisturizing Spray | Na | Xerostomia | Completed | 2019-11-02 | 2019-12-13 | ClinicalTrials.gov |
| NCT03719287 | Study to Estimate the Point Prevalence of Peripheral Intravenous Catheter-relat… | — | Infusion Site Injury | Completed | 2019-01-07 | 2019-10-01 | ClinicalTrials.gov |
| NCT03391960 | Passive Disinfection Cap Compliance Study | Na | Infection, Hospital | Completed | 2018-04-01 | 2018-10-31 | ClinicalTrials.gov |
| NCT03421145 | A Clinical Study to Evaluate Effects of an Oral Rinse on Plaque and Gingivitis | — | Plaque | Completed | 2017-12-17 | 2019-01-17 | ClinicalTrials.gov |
| NCT03298113 | Comparative Study to Assess an Advanced Skin Protectant in the Management of In… | Na | Incontinence-associated Dermatitis | Terminated | 2017-11-17 | 2018-07-10 | ClinicalTrials.gov |
| NCT03681990 | In Vivo Preoperative Skin Preparation Efficacy Study Within a Defined Product C… | Phase2 | Surgical Skin Preparation | Completed | 2017-06-06 | 2017-07-04 | ClinicalTrials.gov |
| NCT03155204 | Comparison of the Pharmacokinetics of Tiotropium Delivered From Test Inhaler Pr… | Early_Phase1 | Healthy | Completed | 2017-04-25 | 2018-03-19 | ClinicalTrials.gov |
| NCT03155178 | In Vivo Preoperative Skin Preparation Persistence Evaluation | Phase2 | Bacterial Recovery of Skin Flora Post-product Application | Completed | 2016-12-05 | 2017-04-25 | ClinicalTrials.gov |
| NCT03302065 | Comparison of the Pharmacokinetics of Tiotropium Delivered From Test Inhaler Pr… | Phase1 | Healthy | Completed | 2016-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02889835 | Clinical Performance of Incremental and Bulk Fill Composites in Class II Restor… | Na | Dental Caries | Completed | 2016-03-22 | 2021-07-03 | ClinicalTrials.gov |
| NCT02676297 | Cross-over Study in Volunteers to Compare the Pharmacokinetics of Tiotropium De… | Phase1 | Healthy | Completed | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02728986 | Cost Evaluation of Venous Leg Ulcers Management | Na | Varicose Ulcer | Completed | 2015-12-17 | 2018-07-01 | ClinicalTrials.gov |
| NCT02627625 | Comparison of the Pharmacokinetics of Tiotropium Delivered From Test Inhaler Pr… | Phase1 | Healthy | Completed | 2015-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02570139 | Clinical Study to Assess a New Barrier Film's Ability to Provide Skin Protectio… | Na | Incontinence Associated Dermatitis | Terminated | 2015-10-01 | 2017-06-23 | ClinicalTrials.gov |
| NCT02258412 | Evaluation of Two Hand Hygiene Products in ICUs | Phase4 | Hand Hygiene Effectiveness | Completed | 2014-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02725788 | Trial Comparing Peripheral I.V. Catheter Complication Rates of Two Different Ca… | Na | Surgery | Terminated | 2014-09-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02195310 | The Use of PrevenaTM on Clean Closed Sternal Midline Incisions in Subjects at H… | Na | Surgical Site Occurences After Sternotomy | Terminated | 2013-11-12 | 2016-10-17 | ClinicalTrials.gov |
| NCT01968356 | In-vivo Efficacy Study of Patient Preoperative Preps | Phase3 | Skin Flora Bacterial Reduction Post-product Application | Terminated | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01968707 | In-vivo Efficacy Study of Patient Pre-operative Preps | Phase3 | Bacterial Reduction on Skin Flora Post-product Application | Completed | 2013-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01500187 | Fluoride Varnish for Treatment of White Spot Lesions | Na | White Spot Lesions | Completed | 2012-02-01 | 2014-03-31 | ClinicalTrials.gov |
| NCT01464294 | Clinical Evaluation of Chairside CAD/CAM Nano-ceramic Restorations | — | Restoration of Posterior Teeth | Terminated | 2011-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01349894 | SNaP Wound Care System Over Skin Cancer Excision Sites and Split Thickness Skin… | — | Split Thickness Skin Graft | Withdrawn | 2011-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01382524 | Peripheral Intravenous Catheter Complication Rate Comparison of Two Different C… | — | Catheter Complications | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01354106 | Adhesive Tape Trauma Evaluation of Two Gentle Tapes | Na | Adhesive Tape Trauma | Completed | 2011-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01313182 | Prevention of Surgical Site Infections: Effectiveness of Nasal Povidone-Iodine … | Phase4 | Surgical Site Infection | Completed | 2011-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01369134 | Clinical Evaluation of a Self-etch Adhesive Using a Selective Etch Technique | — | Dental Caries | Completed | 2011-01-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01278862 | Clinical Evaluation of Lava Digital Veneer System (DVS) Crowns | Na | Decay | Terminated | 2010-11-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01138592 | Pilot Study to Evaluate the Clinical Utility of Auscultation Software at Remote… | — | Auscultation of Heart and Lungs | Completed | 2010-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01096589 | Assessment of 3M Oedema Reduction System in the Treatment of Lymphoedema Compar… | Na | Lymphedema | Completed | 2010-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01290978 | Compare Effect of Surgical Antiseptic Preparations on Incise Drape Adhesion to … | Phase4 | Healthy | Completed | 2010-02-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01013792 | A Comparison of an Investigational Dressing to Tegaderm Matrix Wound Dressing i… | Na | Foot Ulcer, Diabetic | Terminated | 2009-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00854516 | Open Label Clinical Study to Assess the Clinical Safety of a New Compression De… | Na | Peripheral Arterial Vascular Disease | Completed | 2009-02-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00658138 | Clinical Evaluation of 3M™ ESPE™ Adper™ Scotchbond™ SE Self-Etch Adhesive in Cl… | Na | Dental Caries | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00643461 | Clinical Evaluation of Three Dental Adhesive Systems in Class V Restorations | — | Dental Caries | Completed | 2008-04-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00731042 | A Two-week Crossover Evaluation of Two Hand Antiseptic Products on Skin Conditi… | Phase4 | Healthy | Completed | 2008-03-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00558662 | Randomized Clinical Trial (RCT) to Compare the Efficacy of Coban 2 Versus SSB i… | Na | Venous Ulcer | Completed | 2007-11-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00516906 | Clinical Performance of a Chlorhexidine Antimicrobial Dressing | Phase2 | Catheterization | Completed | 2007-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00301496 | Randomized Controlled 8-week Crossover Evaluation of Compression Bandage System… | Na | Venous Ulcer | Completed | 2006-03-01 | 2007-04-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (2% w/w CHG) | Other | Approved | Arthroplasty Replacement, Knee | RECRUITING | NCT07356323 |
| Passive disinfection device | Device | Approved | Infection, Hospital | COMPLETED | NCT03391960 |
| Passive disinfection device | Device | Approved | Infection, Hospital | COMPLETED | NCT03391960 |
| ChloraPrep | Other | Phase PHASE2 | Bacterial Recovery of Skin Flora Post-product Application | COMPLETED | NCT03155178 |
| 3M CHG/IPA Prep | Other | Phase PHASE2 | Bacterial Recovery of Skin Flora Post-product Application | COMPLETED | NCT03155178 |
| ChloraPrep | Other | Phase PHASE2 | Bacterial Recovery of Skin Flora Post-product Application | COMPLETED | NCT03155178 |
| 3M CHG/IPA Prep | Other | Phase PHASE2 | Bacterial Recovery of Skin Flora Post-product Application | COMPLETED | NCT03155178 |
| tiotropium | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02676297 |
| Tiotropium | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02627625 |
| Wound and per-wound assessments While using Device | Device | Approved | WOUNDS INJURIES | WITHDRAWN | NCT05748392 |
| Normal saline | Other | Phase PHASE3 | Surgical Skin Preparation | COMPLETED | NCT04756154 |
| CHG/IPA Surgical skin preparation | Other | Phase PHASE3 | Surgical Skin Preparation | COMPLETED | NCT04756154 |
| Normal saline | Other | Phase PHASE3 | Surgical Skin Preparation | COMPLETED | NCT04756154 |
| CHG/IPA Surgical skin preparation | Other | Phase PHASE3 | Surgical Skin Preparation | COMPLETED | NCT04756154 |
| Standard Silver-containing Dressing | Other | Approved | Surgical Wound | TERMINATED | NCT04712019 |
| Closed Incision Negative Pressure Therapy (ciNPT) | Drug | Approved | Surgical Wound | TERMINATED | NCT04712019 |
| Anti-plaque | Other | Approved | Oral Mucosal Disorder | TERMINATED | NCT04601103 |
| High SLS toothpaste | Other | Approved | Oral Mucosal Disorder | TERMINATED | NCT04601103 |
| Medium SLS toothpaste | Other | Approved | Oral Mucosal Disorder | TERMINATED | NCT04601103 |
| No SLS toothpaste | Other | Approved | Oral Mucosal Disorder | TERMINATED | NCT04601103 |
| Water | Other | Preclinical | Plaque | COMPLETED | NCT03421145 |
| PerioShield™ Oral Health Rinse | Other | Preclinical | Plaque | COMPLETED | NCT03421145 |
| Vehicle Control Oral Rinse | Other | Preclinical | Plaque | COMPLETED | NCT03421145 |
| 3M™ Oral Rinse | Other | Preclinical | Plaque | COMPLETED | NCT03421145 |
| Bulk Fill Flowable Restorative | Other | Approved | Dental Caries | COMPLETED | NCT02889835 |
| Supreme Flowable Restorative | Other | Approved | Dental Caries | COMPLETED | NCT02889835 |
| Supreme Universal Restorative | Other | Approved | Dental Caries | COMPLETED | NCT02889835 |
| Biotene Moisturizing Mouth Spray to 3M Dry Mouth Moisturizing Spray | Other | Approved | Xerostomia | COMPLETED | NCT04186806 |
| 3M Dry Mouth Moisturizing Spray to Biotene Moisturizing Mouth Spray | Other | Approved | Xerostomia | COMPLETED | NCT04186806 |
| 3M CHG/IPA Prep | Other | Phase PHASE2 | Surgical Skin Preparation | COMPLETED | NCT03681990 |
| ConvaTec Sensi-Care Protective Barrier | Other | Approved | Incontinence Associated Dermatitis | TERMINATED | NCT02570139 |
| Cavilon Advanced Skin Protectant | Other | Approved | Incontinence Associated Dermatitis | TERMINATED | NCT02570139 |
| Conventional sterile wound dressings | Other | Approved | Surgical Site Occurences After Sternotomy | TERMINATED | NCT02195310 |
| Prevena™ Incision Management System | Other | Approved | Surgical Site Occurences After Sternotomy | TERMINATED | NCT02195310 |
| Conventional sterile wound dressings | Other | Approved | Surgical Site Occurences After Sternotomy | TERMINATED | NCT02195310 |
| Prevena™ Incision Management System | Other | Approved | Surgical Site Occurences After Sternotomy | TERMINATED | NCT02195310 |
| 3M CHG/IPA Prep Tint 26-mL | Other | Phase PHASE3 | Bacterial Reduction on Skin Flora Post-product Application | COMPLETED | NCT01968707 |
| 3M CHG/IPA Prep Tint 10.5-mL | Other | Phase PHASE3 | Bacterial Reduction on Skin Flora Post-product Application | COMPLETED | NCT01968707 |
| Normal saline | Other | Phase PHASE3 | Bacterial Reduction on Skin Flora Post-product Application | COMPLETED | NCT01968707 |
| ChloraPrep Hi-Lite Orange | Other | Phase PHASE3 | Bacterial Reduction on Skin Flora Post-product Application | COMPLETED | NCT01968707 |
| Saline | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| ChloraPrep | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| 3M CHG/IPA Prep Tint | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| 3M CHG/IPA Prep Colorless | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| Saline | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| ChloraPrep | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| 3M CHG/IPA Prep Tint | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| 3M CHG/IPA Prep Colorless | Other | Phase PHASE3 | Skin Flora Bacterial Reduction Post-product Application | TERMINATED | NCT01968356 |
| Pediagel | Other | Approved | White Spot Lesions | COMPLETED | NCT01500187 |
| Vanish Varnish | Other | Approved | White Spot Lesions | COMPLETED | NCT01500187 |
| Adper Easy Bond Self-etch dental adhesive | Other | Preclinical | Dental Caries | COMPLETED | NCT01369134 |
| Skin Trauma | Other | Approved | Adhesive Tape Trauma | COMPLETED | NCT01354106 |
| SNaP® Wound Care System | Other | Preclinical | Split Thickness Skin Graft | WITHDRAWN | NCT01349894 |
| DuraPrep | Other | Phase PHASE4 | Healthy | COMPLETED | NCT01290978 |
| ChloraPrep | Other | Phase PHASE4 | Healthy | COMPLETED | NCT01290978 |
| Comprilan | Other | Approved | Lymphedema | COMPLETED | NCT01096589 |
| 3M Coban 2 (Compression System) | Other | Approved | Lymphedema | COMPLETED | NCT01096589 |
| Comprilan | Other | Approved | Lymphedema | COMPLETED | NCT01096589 |
| 3M Coban 2 (Compression System) | Other | Approved | Lymphedema | COMPLETED | NCT01096589 |
| Wound Dressing | Other | Approved | Foot Ulcer, Diabetic | TERMINATED | NCT01013792 |
| A new treatment approach is to have an effective working pressure combined with a low resting pressure. | Drug | Approved | Peripheral Arterial Vascular Disease | COMPLETED | NCT00854516 |
| A new treatment approach is to have an effective working pressure combined with a low resting pressure. | Drug | Approved | Peripheral Arterial Vascular Disease | COMPLETED | NCT00854516 |
| 3M ESPE Adper Scotchbond 1XT | Other | Approved | Dental Caries | COMPLETED | NCT00658138 |
| 3M ESPE Adper Scotchbond SE | Other | Approved | Dental Caries | COMPLETED | NCT00658138 |
| Adhesive C | Other | Preclinical | Dental Caries | COMPLETED | NCT00643461 |
| Adhesive B | Other | Preclinical | Dental Caries | COMPLETED | NCT00643461 |
| Adhesive A | Other | Preclinical | Dental Caries | COMPLETED | NCT00643461 |
| SSB | Other | Approved | Venous Ulcer | COMPLETED | NCT00558662 |
| Coban 2 | Other | Approved | Venous Ulcer | COMPLETED | NCT00558662 |
| Coban 2 Layer Compression System | Other | Approved | Venous Ulcer | COMPLETED | NCT00301496 |
| Alcohol hand sanitizer foam | Other | Phase PHASE4 | Hand Hygiene Effectiveness | COMPLETED | NCT02258412 |
| hand antiseptic with CHG and alcohol | Other | Phase PHASE4 | Hand Hygiene Effectiveness | COMPLETED | NCT02258412 |
| Standard PIV Dressing | Other | Approved | Surgery | TERMINATED | NCT02725788 |
| New PIV Dressing | Other | Approved | Surgery | TERMINATED | NCT02725788 |
| Standard PIV Dressing | Other | Approved | Surgery | TERMINATED | NCT02725788 |
| New PIV Dressing | Other | Approved | Surgery | TERMINATED | NCT02725788 |
| Transparent Adhesive Dressing | Other | Phase PHASE2 | Catheterization | COMPLETED | NCT00516906 |
| Chlorhexidine gluconate | Other | Phase PHASE2 | Catheterization | COMPLETED | NCT00516906 |
| Transparent Adhesive Dressing | Other | Phase PHASE2 | Catheterization | COMPLETED | NCT00516906 |
| Chlorhexidine gluconate | Other | Phase PHASE2 | Catheterization | COMPLETED | NCT00516906 |
| Tiotropium | Other | Phase PHASE1 | Healthy | COMPLETED | NCT03302065 |
| IAD Hospital Standard Care | Other | Approved | Incontinence-associated Dermatitis | TERMINATED | NCT03298113 |
| Cavilon Advanced Skin Protectant | Other | Approved | Incontinence-associated Dermatitis | TERMINATED | NCT03298113 |
| tiotropium pMDI | Other | Phase EARLY_PHASE1 | Healthy | COMPLETED | NCT03155204 |
| Coban2 | Other | Approved | Varicose Ulcer | COMPLETED | NCT02728986 |
| Profore | Other | Approved | Varicose Ulcer | COMPLETED | NCT02728986 |
| Coban2 | Other | Approved | Varicose Ulcer | COMPLETED | NCT02728986 |
| Profore | Other | Approved | Varicose Ulcer | COMPLETED | NCT02728986 |
| Milled nano-composite restorations | Other | Preclinical | Restoration of Posterior Teeth | TERMINATED | NCT01464294 |
| Milled ceramic restorations | Other | Preclinical | Restoration of Posterior Teeth | TERMINATED | NCT01464294 |
| Milled nano-composite restorations | Other | Preclinical | Restoration of Posterior Teeth | TERMINATED | NCT01464294 |
| Milled ceramic restorations | Other | Preclinical | Restoration of Posterior Teeth | TERMINATED | NCT01464294 |
| 3M Skin and Nasal Antiseptic | Other | Phase PHASE4 | Surgical Site Infection | COMPLETED | NCT01313182 |
| mupirocin calcium ointment, 2% | Other | Phase PHASE4 | Surgical Site Infection | COMPLETED | NCT01313182 |
| 3M Skin and Nasal Antiseptic | Other | Phase PHASE4 | Surgical Site Infection | COMPLETED | NCT01313182 |
| mupirocin calcium ointment, 2% | Other | Phase PHASE4 | Surgical Site Infection | COMPLETED | NCT01313182 |
| Conventional Veneer | Other | Approved | Decay | TERMINATED | NCT01278862 |
| DVS veneer | Other | Approved | Decay | TERMINATED | NCT01278862 |
| Purell Surgical Scrub | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00731042 |
| Avagard | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00731042 |
| Purell Surgical Scrub | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00731042 |
| Avagard | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00731042 |
| Chairside zirconia crowns (3M) | Other | Approved | Dental Cements | COMPLETED | NCT04279574 |
| Lithium disilicate onlays (IPS emaxCAD/Ivoclar) | Other | Approved | Dental Cements | COMPLETED | NCT04279574 |
| Vitrebond™ Pulp Protect Liner/Base | Other | Approved | Dental Caries | NOT_YET_RECRUITING | NCT07231237 |
| Vitrebond™ Plus (comparator) | Other | Approved | Caries, Dental | NOT_YET_RECRUITING | NCT07261137 |
| Vitrebond™ Pulp Protect Liner/Base | Other | Approved | Caries, Dental | NOT_YET_RECRUITING | NCT07261137 |
| 3M™ V.A.C.® Peel and Place Dressing | Other | Approved | Wound | RECRUITING | NCT06625385 |
| 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (2% w/w CHG) | Other | Approved | Arthroplasty Replacement, Knee | RECRUITING | NCT07356323 |
| 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (2% w/w CHG) | Other | Approved | Arthroplasty Replacement, Knee | RECRUITING | NCT07356323 |
| Scotchbond Universal Adhesive | Other | Approved | Class V Non-carious Cervical Dental Lesions | COMPLETED | NCT05361746 |
| Scotchbond Universal Plus Adhesive | Other | Approved | Class V Non-carious Cervical Dental Lesions | COMPLETED | NCT05361746 |