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)

TALLADIUM TILITE CERAMIC ALLOY

K-Number: K894085 · 1989-12-20

ApplicantTalladium, Inc.
Decision Date1989-12-20
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TALLADIUM TILITE CERAMIC ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Talladium, Inc.. It received FDA 510(k) clearance on 1989-12-20 under 510(k) number K894085. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TALLADIUM TILITE CERAMIC ALLOY?

TALLADIUM TILITE CERAMIC ALLOY is a medical device that received FDA 510(k) clearance on 1989-12-20. The listed applicant is Talladium, Inc.. The 510(k) number is K894085.

When did TALLADIUM TILITE CERAMIC ALLOY receive FDA 510(k) clearance?

TALLADIUM TILITE CERAMIC ALLOY received FDA 510(k) clearance on 1989-12-20, under 510(k) number K894085.

Who is the listed applicant for TALLADIUM TILITE CERAMIC ALLOY?

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

What is the FDA product code for TALLADIUM TILITE CERAMIC ALLOY?

The FDA product code for TALLADIUM TILITE CERAMIC ALLOY is EJH.

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 Talladium, 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.

K152023Luminesse Shaded Zirconia SZK100232LUMINESSE ZR BLANKS

Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K032136WIROBOND CBego U.S.A.

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.

↑