COLLAGEN DENTAL MEMBRANE V
K-Number: K100156 · 2010-08-11
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Device Summary
Frequently Asked Questions
What is the COLLAGEN DENTAL MEMBRANE V?
COLLAGEN DENTAL MEMBRANE V is a medical device that received FDA 510(k) clearance on 2010-08-11. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K100156.
When did COLLAGEN DENTAL MEMBRANE V receive FDA 510(k) clearance?
COLLAGEN DENTAL MEMBRANE V received FDA 510(k) clearance on 2010-08-11, under 510(k) number K100156.
Who is the listed applicant for COLLAGEN DENTAL MEMBRANE V?
The FDA 510(k) record lists Collagen Matrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLAGEN DENTAL MEMBRANE V?
The FDA product code for COLLAGEN DENTAL MEMBRANE V is NPL.
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 Collagen Matrix, 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: NPL)
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.
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