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FDA 510(k)

COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN

K-Number: K110600 · 2011-07-29

ApplicantCollagen Matrix, Inc.
Decision Date2011-07-29
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2011-07-29 under 510(k) number K110600. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN?

COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN is a medical device that received FDA 510(k) clearance on 2011-07-29. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K110600.

When did COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN receive FDA 510(k) clearance?

COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN received FDA 510(k) clearance on 2011-07-29, under 510(k) number K110600.

Who is the listed applicant for COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN?

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 MAMBRANE - PORCINE TYPE I COLLAGEN?

The FDA product code for COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN is NPL.

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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.

K251191Collagen Dura Regeneration Membrane - RepairK243071Bovine Dermis Collagen Dermal MatrixK242302RejuvaKnee™ Collagen Meniscus ImplantK233203Soft Tissue Augmentation Resorbable MatrixK240424Mineral Collagen Composite Bioactive Moldable Bone Graft MatrixK231942Mineral Collagen Composite Bioactive Extra Moldable

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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.

K242817Jason membraneBotiss Biomaterials GmbHK250512Augmented Gingival MatrixNeo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.K252253Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide®Geistlich Pharma AGK251062Geistlich Bio-Gide; Geistlich Bio-Gide® Shape; Geistlich Bio-Gide® Compressed; Geistlich Bio-Gide® Forte; Geistlich Bio-Gide® Perio; Geistlich Combi-Kit Collagen®; Geistlich Perio-System Combi PackGeistlich Pharma AGK250833SwissMembrane X; SwissMembrane X SocketGeistlich Pharma AGK233203Soft Tissue Augmentation Resorbable MatrixCollagen Matrix, Inc.

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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