DynaMesh

Hernia Mesh made of 100% Polyvinylidene Fluorid

Registry build 21.09.26
1manufacturer
45catalogue numbers in this listing

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code FTL
Manufacturer City Province Registered as Device types
Shanghai Suokang Medical Implants Co., Ltd. Shang Hai Shanghai Manufacturer 2

Record

Regulatory record for DynaMesh
Listed by FEG Textiltechnik Forschungs- und Entwicklungsges. mbH
FDA product code FTL
Device type Mesh, Surgical, Polymeric
Device class Class 2
Regulation 21 CFR 878.3300
Premarket notification Exempt
Record published 2017-05-08
Record revised 2025-08-18 (version 6)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Cardboard box of 5, cardboard box of 2, cardboard box of 3

Catalogue Numbers

Catalogue numbers for DynaMesh
Catalogue number Size Status
VENTRAL In distribution
VENTRAL In distribution
PP light 1515 In distribution
CICAT 1010 In distribution
PP light 0611 In distribution
VENTRAL In distribution
VENTRAL In distribution
PP light 0630 In distribution
PP light 1015 In distribution
VENTRAL In distribution
CICAT 2030 In distribution
PP standard 1015 In distribution
VENTRAL In distribution
PP light 0605 In distribution
PP standard 2030 In distribution
VENTRAL In distribution
PP standard 0605 In distribution
VENTRAL In distribution
PP light 2030 In distribution
VENTRAL In distribution
VENTRAL In distribution
VENTRAL In distribution
PP light 0715 In distribution
CICAT 2715 In distribution
CICAT 0010 In distribution
CICAT 1525 In distribution
VENTRAL In distribution
VENTRAL In distribution
CICAT 4020 In distribution
VENTRAL In distribution
VENTRAL In distribution
PP standard 0611 In distribution
PP standard 0630 In distribution
CICAT 4010 In distribution
CICAT 1035 In distribution
VENTRAL In distribution
VENTRAL In distribution
PP standard 3045 In distribution
PP standard 0715 In distribution
PP standard 3030 In distribution
PP standard 1515 In distribution
VENTRAL In distribution
CICAT 3045 In distribution
PP light 3045 In distribution
PP light 3030 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Technical Products Technical Products, Inc. 143
Parietex Sofradim Production 82
Symbotex Sofradim Production 35
Silicone Sheeting Reinforced Bentec Medical OpCo, LLC. 33
Parietene Sofradim Production 32
C-QUR Atrium Medical Corporation 31
ProGrip Sofradim Production 31
Silicone Sheeting Non-Reinforced Bentec Medical OpCo, LLC. 31
Prolite Atrium Medical Corporation 31
Gore Seamguard Bioabsorbable Staple Line Reinforce W. L. Gore & Associates, Inc. 30
Surgimesh®wn Aspide Medical 28
Bard Davol Inc. 27

Showing 12 of 148. All products under Mesh, Surgical, Polymeric

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P990028 2003-12-04 FOCALSEAL-L SYNTHETIC ABSORBABLE SEALANT Genzyme Corporation

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