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)

IONOSIT BASE LINER

K-Number: K935689 · 1994-01-21

ApplicantForemost Dental Mfg., Co.
Decision Date1994-01-21
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IONOSIT BASE LINER is the device name listed in this FDA 510(k) record. The listed applicant is Foremost Dental Mfg., Co.. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K935689. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IONOSIT BASE LINER?

IONOSIT BASE LINER is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Foremost Dental Mfg., Co.. The 510(k) number is K935689.

When did IONOSIT BASE LINER receive FDA 510(k) clearance?

IONOSIT BASE LINER received FDA 510(k) clearance on 1994-01-21, under 510(k) number K935689.

Who is the listed applicant for IONOSIT BASE LINER?

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

What is the FDA product code for IONOSIT BASE LINER?

The FDA product code for IONOSIT BASE LINER is EBD.

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

Related Devices (Code: EBD)

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.

K254091GLOSSY COAT (15ML)YAMAHACHI DENTAL MFG., Co.K250804ID LIGHT CURE SYSTEMId Korea Co., Ltd.K240735visio.lign color, visio.lign shieldBredent GmbH & Co. KGK223365RODIN Palette Naturalizing KitBelport Company, Inc., Gingi-PakK211854VITA Akzent LCVita Zahnfabrik GmbH H Rauter & COK162408Nano Varnish, Plaquit, Lightpaint on SurfaceDreve Dentamid GmbH

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.

↑