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)

ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS

K-Number: K890712 · 1989-04-25

Decision Date1989-04-25
Product CodeEBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Dental Products, Inc.. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K890712. The device is classified under product code EBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS?

ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Advantage Dental Products, Inc.. The 510(k) number is K890712.

When did ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS receive FDA 510(k) clearance?

ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS received FDA 510(k) clearance on 1989-04-25, under 510(k) number K890712.

Who is the listed applicant for ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS?

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

What is the FDA product code for ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS?

The FDA product code for ADVANTAGE DENTAL CUST DENT IMPRESS/BASEPLATE TRAYS is EBH.

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.

Other records listing Advantage Dental Products, 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.

Related Devices (Code: EBH)

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.

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.

↑