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)

STEADFAST DENTURE ADHESIVE CREAM

K-Number: K895818 · 1990-04-03

ApplicantStiefel Research Institute, Inc.
Decision Date1990-04-03
Product CodeKOT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STEADFAST DENTURE ADHESIVE CREAM is the device name listed in this FDA 510(k) record. The listed applicant is Stiefel Research Institute, Inc.. It received FDA 510(k) clearance on 1990-04-03 under 510(k) number K895818. 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 STEADFAST DENTURE ADHESIVE CREAM?

STEADFAST DENTURE ADHESIVE CREAM is a medical device that received FDA 510(k) clearance on 1990-04-03. The listed applicant is Stiefel Research Institute, Inc.. The 510(k) number is K895818.

When did STEADFAST DENTURE ADHESIVE CREAM receive FDA 510(k) clearance?

STEADFAST DENTURE ADHESIVE CREAM received FDA 510(k) clearance on 1990-04-03, under 510(k) number K895818.

Who is the listed applicant for STEADFAST DENTURE ADHESIVE CREAM?

The FDA 510(k) record lists Stiefel Research Institute, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEADFAST DENTURE ADHESIVE CREAM?

The FDA product code for STEADFAST DENTURE ADHESIVE CREAM 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 Stiefel Research Institute, 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.

K914591L.C.S. 2000 SYSTEMK910216STEADFAST DENTURE ADHESIVE POWDERK895817HERMAL WOUND CARE KITK896724CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU.K893996CUSIS ULTRASOUND SKIN IMAGING SYSTEM

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 GetzK884357PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEMPrecision Dynamics Corp.K872225SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDERBlock Drug Company, Inc.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.

↑