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)

TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS)

K-Number: K896501 · 1990-02-09

ApplicantLeach and Dillon Co., Inc.
Decision Date1990-02-09
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS) is the device name listed in this FDA 510(k) record. The listed applicant is Leach and Dillon Co., Inc.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K896501. 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 TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS)?

TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS) is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Leach and Dillon Co., Inc.. The 510(k) number is K896501.

When did TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS) receive FDA 510(k) clearance?

TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS) received FDA 510(k) clearance on 1990-02-09, under 510(k) number K896501.

Who is the listed applicant for TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS)?

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

What is the FDA product code for TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS)?

The FDA product code for TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS) 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 Leach and Dillon Co., 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.

K903538WIRON 99 DENTAL CASTING ALLOYK903537250 SL DENTAL CASTING ALLOYK895059HIGH FUSING YELLOW CERAMIC SOLDERK895058HIGH FUSING WHITE CERAMIC SOLDERK903484SELECT 20, DENTAL ALLOYK902372SILVER-FREE CERAMIC SOLDER (SFCS)

View all 31 devices →

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.

↑