Ethicon Physiomesh

Physiomesh Flexible Composite Mesh

Registry build 21.09.26
1manufacturer
22catalogue 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 Ethicon Physiomesh
Listed by Johnson & Johnson Medical GmbH, Germany
FDA product code FTL
Device type Mesh, Surgical, Polymeric
Device class Class 2
Regulation 21 CFR 878.3300
Establishment Contract manufacturer, Manufacturer
Record published 2019-01-25
Record revised 2026-03-31 (version 9)

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 Storage environment temperature up to 30 °C
Distribution end date 2026-04-30

Catalogue Numbers

Catalogue numbers for Ethicon Physiomesh
Catalogue number Size Status
OPHY1525 In distribution
OPHY2030 In distribution
OPHY1010 In distribution
OPHY1215 In distribution
OPHY2536 In distribution
OPHY1520 In distribution
OPHY1525 Withdrawn
PHY1520R Withdrawn
PHY2030R Withdrawn
OPHY2536 Withdrawn
PHY3050R Withdrawn
OPHY1010 Withdrawn
PHY2025V Withdrawn
PHY1520V Withdrawn
PHY0715R Withdrawn
OPHY1215 Withdrawn
PHY1515Q Withdrawn
OPHY2030 Withdrawn
PHY2535V Withdrawn
PHY3035R Withdrawn
OPHY1520 Withdrawn
PHY1015V Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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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

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