DynaMatrix Plus

DynaMatrix Plus Extracellular Membrane

Registry build 21.09.26
2manufacturers in China registered for this device type
6catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code NPL
Manufacturer City Province Registered as Device types
Beijing Biosis Healing Biological Technology Co., Ltd. Beijing Beijing Manufacturer 7
NEO Modulus (Suzhou) Medical SCI-Tech Co., Ltd. Suzhou Jiangsu Manufacturer 1

Record

Regulatory record for DynaMatrix Plus
Listed by Cook Biotech, Inc., United States
FDA product code NPL
Device type Barrier, Animal Source, Intraoral
Device class Class 2
Regulation 21 CFR 872.3930
Establishment Contract manufacturer, Manufacturer
510(k) K082058
Record published 2015-11-03
Record revised 2026-07-20 (version 10)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store in a clean place at room temperature. Do not place in freezer. Avoid excessive heat. Keep dry.

Catalogue Numbers

Catalogue numbers for DynaMatrix Plus
Catalogue number Size Status
G56900 In distribution
G56902 In distribution
G56899 In distribution
G56901 In distribution
G56903 In distribution
G56898 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neocirrus NEO Modulus (Suzhou) Medical SCI-Tech Co., Ltd. 18
Gibson Healthcare Benco Dental Supply Co. 18
Endoform™ Dental Membrane Aroa Biosurgery Ltd 12
Ousia bioADAPT Ace Surgical Supply Co., Inc. 9
GuidOss Nibec Co Ltd 9
RCM6 Resorbable Collagen Membrane Ace Surgical Supply Co., Inc. 9
Ousia bioMAINTAIN Ace Surgical Supply Co., Inc. 9
Genoss Collagen Membrane Genoss Co., Ltd. 9
bioMAINTAIN Collagen Matrix, Inc. 9
Salvin Dental Specialties Salvin Dental Specialties, LLC 8
THE Cover Purgo Biologics Inc. 8
PerioMatrix Collagen Matrix, Inc. 7

Showing 12 of 132. All products under Barrier, Animal Source, Intraoral

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K161762 2017-01-13
K082058 2008-10-02
K010952 2002-06-10

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer