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FDA 510(k)

COMFOR-DENT DENTURE LINER

K-Number: K910795 · 1991-07-11

Decision Date1991-07-11
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMFOR-DENT DENTURE LINER is the device name listed in this FDA 510(k) record. The listed applicant is Comfort Acrylics Co.. It received FDA 510(k) clearance on 1991-07-11 under 510(k) number K910795. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFOR-DENT DENTURE LINER?

COMFOR-DENT DENTURE LINER is a medical device that received FDA 510(k) clearance on 1991-07-11. The listed applicant is Comfort Acrylics Co.. The 510(k) number is K910795.

When did COMFOR-DENT DENTURE LINER receive FDA 510(k) clearance?

COMFOR-DENT DENTURE LINER received FDA 510(k) clearance on 1991-07-11, under 510(k) number K910795.

Who is the listed applicant for COMFOR-DENT DENTURE LINER?

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

What is the FDA product code for COMFOR-DENT DENTURE LINER?

The FDA product code for COMFOR-DENT DENTURE LINER is EBI.

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 Comfort Acrylics Co. 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: EBI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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