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)

UNI-BITE DENTAL X-RAY FILM HOLDER

K-Number: K813378 · 1982-01-29

ApplicantRinn Corp.
Decision Date1982-01-29
Product CodeEGZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNI-BITE DENTAL X-RAY FILM HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Rinn Corp.. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K813378. The device is classified under product code EGZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNI-BITE DENTAL X-RAY FILM HOLDER?

UNI-BITE DENTAL X-RAY FILM HOLDER is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Rinn Corp.. The 510(k) number is K813378.

When did UNI-BITE DENTAL X-RAY FILM HOLDER receive FDA 510(k) clearance?

UNI-BITE DENTAL X-RAY FILM HOLDER received FDA 510(k) clearance on 1982-01-29, under 510(k) number K813378.

Who is the listed applicant for UNI-BITE DENTAL X-RAY FILM HOLDER?

The FDA 510(k) record lists Rinn Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNI-BITE DENTAL X-RAY FILM HOLDER?

The FDA product code for UNI-BITE DENTAL X-RAY FILM HOLDER is EGZ.

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 Rinn Corp. 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.

K932134RINN UNIVERSAL COLLIMATORK913885RINN E-Z CAPPERK828605BEAM LIMITING DEVICEK772313X-RAY CO-ORDINATOR

Related Devices (Code: EGZ)

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.

K913168SALIBAGNix Co. , Ltd.K913160ID-TABNix Co. , Ltd.K890355DENTAL X-RAY BITE BLOCKBite-A-BlockK853451TROLL-BITETrollplast, Inc.K852170EZX YELLOW, BLUE OR ORANGEStrong MarketingK853005S.S. WHITE DENTAL X-RAY FILM HOLDER & ALIGNING ARMThe S. S. White Co.

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.

↑