Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER

K-Number: K872225 · 1987-06-30

ApplicantBlock Drug Company, Inc.
Decision Date1987-06-30
Product CodeKOT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Block Drug Company, Inc.. It received FDA 510(k) clearance on 1987-06-30 under 510(k) number K872225. The device is classified under product code KOT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER?

SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER is a medical device that received FDA 510(k) clearance on 1987-06-30. The listed applicant is Block Drug Company, Inc.. The 510(k) number is K872225.

When did SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER receive FDA 510(k) clearance?

SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER received FDA 510(k) clearance on 1987-06-30, under 510(k) number K872225.

Who is the listed applicant for SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER?

The FDA 510(k) record lists Block Drug Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER?

The FDA product code for SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER is KOT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Block Drug Company, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K945462SUPER POLI-GRIP DENTURE ADHESIVE CREAMK935925VISION PROPHY PASTE WITH FLUORIDEK933893VISION PROPHY PASTE WITHOUT FLUORIDEK884533SENSODYNE SEALANT DENTIN CONDITIONING SYSTEMK881974PROFICIENT(TM) PROPHYLAXIS ANGLEK862876NEW SUPER POLI-GRIP DENTURE ADHESIVE CREAM

View all 10 devices →

Related Devices (Code: KOT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K945462SUPER POLI-GRIP DENTURE ADHESIVE CREAMBlock Drug Company, Inc.K941365MPI DENTURE ADHESIVE FILM SEALSMedical Polymers, Inc.K903568SUPER STRENGTH DENTURE ADHESIVE CREAMTeledyne GetzK895818STEADFAST DENTURE ADHESIVE CREAMStiefel Research Institute, Inc.K884357PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEMPrecision Dynamics Corp.K854430RIGIDENT CREAMArmkel, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑