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)

MUCOGRAFT COLLAGEN MATRIX

K-Number: K073711 · 2008-05-30

ApplicantEd. Geistlich Soehne AG Fuer Chemische Industrie
Decision Date2008-05-30
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MUCOGRAFT COLLAGEN MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Ed. Geistlich Soehne AG Fuer Chemische Industrie. It received FDA 510(k) clearance on 2008-05-30 under 510(k) number K073711. 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 MUCOGRAFT COLLAGEN MATRIX?

MUCOGRAFT COLLAGEN MATRIX is a medical device that received FDA 510(k) clearance on 2008-05-30. The listed applicant is Ed. Geistlich Soehne AG Fuer Chemische Industrie. The 510(k) number is K073711.

When did MUCOGRAFT COLLAGEN MATRIX receive FDA 510(k) clearance?

MUCOGRAFT COLLAGEN MATRIX received FDA 510(k) clearance on 2008-05-30, under 510(k) number K073711.

Who is the listed applicant for MUCOGRAFT COLLAGEN MATRIX?

The FDA 510(k) record lists Ed. Geistlich Soehne AG Fuer Chemische Industrie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUCOGRAFT COLLAGEN MATRIX?

The FDA product code for MUCOGRAFT COLLAGEN MATRIX 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.

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 Ed. Geistlich Soehne AG Fuer Chemische Industrie 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.

K092428BIO-OSS COLLAGENK061244MUCOGRAFTK050446BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONEK042197BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE REGENERATIONK012423MUCOGRAFT

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.

↑