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Device Explorer · FDA GUDID · GMDN 58709

Collagen dental regeneration membrane

A sterile bioabsorbable material intended to be used to aid in the regeneration of tooth support, lost due to periodontal disease or trauma, and to regenerate bone defects around implants and at sites intended for implant placement, by acting as a barrier to p

US‑registered devices460in commercial distribution
Companies25labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription95%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Collagen Matrix, Inc.17638%
Ace Surgical Supply Co., Inc.368%
Dsm Biomedical, Inc.245%
Hyundai Bioland Co., Ltd.225%
Geistlich Pharma Ag204%
Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.184%
Benco Dental Supply Co.184%
Salvin Dental Specialties, Llc163%

Top labelers

CompanyDevicesShare
Collagen Matrix, Inc.17638%
Ace Surgical Supply Co., Inc.368%
Dsm Biomedical, Inc.245%
Hyundai Bioland Co., Ltd.225%
Geistlich Pharma Ag204%
Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.184%
Benco Dental Supply Co.184%
Salvin Dental Specialties, Llc163%
Datum Dental Ltd153%
Genoss Co., Ltd.143%
Nibec Co., Ltd.123%
Osteogenics Biomedical Inc112%

Company = labeler of record on GUDID. 25 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Bionnovation Gide XPGeistlich Bio-Gide®SwissMembrane X D-LineGeistlich Bio-Gide® ForteGeistlich Bio-Gide® ShapeGeistlich Bio-Gide® CompressedGeistlich Bio-Gide® PerioGeistlich Combi-Kit CollagenMIS 4BONEOSSIX® PLUSOSSIX Agile™OSSIX® BreezeOSSIX® VOLUMAXNeocirrusSYMBIOS®N/A

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
NPLBarrier, Animal Source, Intraoral404
NPLBarrier, animal source, intraoral70
LYCBone grafting material, synthetic10
NPMBone Grafting Material, Animal Source1
LYCBone Grafting Material, Synthetic1

GMDN & GCC registration

  • GMDN code 58709 · implantable
  • Single‑use 100% · sterile 100% · Rx‑only 95% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Width (Millimeter) · 246Length (Millimeter) · 229Height (Millimeter) · 19Width (Centimeter) · 15Length (Centimeter) · 12Height (Centimeter) · 3

Use these as the dimensions to specify in a tender line.

No closely related category with 50+ devices.

How many collagen dental regeneration membrane products are registered in the US?

460 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Collagen dental regeneration membrane", from 25 companies. The largest labeler is Collagen Matrix, Inc. with 38% of records.

Which FDA product codes apply?

NPL (Barrier, Animal Source, Intraoral), NPL (Barrier, animal source, intraoral), LYC (Bone grafting material, synthetic), NPM (Bone Grafting Material, Animal Source)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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