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)

DENTAL MOUTH PROP.

K-Number: K802696 · 1980-11-12

ApplicantTrident Dental, Inc.
Decision Date1980-11-12
Product CodeJXL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DENTAL MOUTH PROP. is the device name listed in this FDA 510(k) record. The listed applicant is Trident Dental, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802696. The device is classified under product code JXL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL MOUTH PROP.?

DENTAL MOUTH PROP. is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Trident Dental, Inc.. The 510(k) number is K802696.

When did DENTAL MOUTH PROP. receive FDA 510(k) clearance?

DENTAL MOUTH PROP. received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802696.

Who is the listed applicant for DENTAL MOUTH PROP.?

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

What is the FDA product code for DENTAL MOUTH PROP.?

The FDA product code for DENTAL MOUTH PROP. is JXL.

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 Trident Dental, 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.

K800866ROYALK800865WINDSOR

Related Devices (Code: JXL)

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.

K221469PATI (Protector Against Tongue Injury)Neurovice, LLCK201309ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size MediumMecta CorporationK172978SurgeoBiteSurgovations, LLCK050188EPIGUARDEpisafe Medical Devices, Ltd.K992269VENTIL-A ORAL PROTECTORSomatics, Inc.K960663UNIVERSAL BITE BLOCKB&B Medical Technologies, Inc.

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.

↑