Covamax

Collagen Guided Healing Membrane

Registry build 21.09.26
2manufacturers in China registered for this device type
3catalogue numbers in this listing
1recall

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 Covamax
Listed by Dilon Technologies France SAS, France
FDA product code NPL
Device type Barrier, Animal Source, Intraoral
Device class Class 2
Regulation 21 CFR 872.3930
Establishment Repacker / relabeller, Manufacturer
Record published 2016-02-22
Record revised 2023-10-04 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Dry place away from humidity; Handling environment temperature 2 to 30 °C; Storage environment temperature 2 to 30 °C
Sizes Length 25 to 40 mm; width 15 to 30 mm
Distribution end date 2019-05-21

Catalogue Numbers

Catalogue numbers for Covamax
Catalogue number Size Status
MCG 11 12 AA Length 25 mm Withdrawn
MCG 12 23 AA Length 30 mm Withdrawn
MCG 13 34 AA Length 40 mm Withdrawn

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

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2016-12-02 Class II Nonconforming Material/Component Lack of sterility assurance 1,682 units 2017-05-05

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