Ultrapro

Ultrapro MONOCRYL™-PROLENE™- COMPOSITE Poliglecaprone 25/Polypropylene Sterile, Synthetic, Partially Absorbable Mesh

Registry build 21.09.26
1manufacturer
21catalogue 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 Ultrapro
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 2019-09-24
Record revised 2025-03-12 (version 8)

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 25 °C
Packaging Box of 3, box of 6, box of 2, box
Distribution end date 2026-04-30

Catalogue Numbers

Catalogue numbers for Ultrapro
Catalogue number Size Status
UMS3 In distribution
UMR3 In distribution
UPPL6 In distribution
UHSL In distribution
UML1 In distribution
UPPL2 In distribution
UPPM2 In distribution
UPPS6 In distribution
UPPS1 In distribution
UHSM In distribution
UPPM6 In distribution
UPPM1 In distribution
UMM3 In distribution
UPPS2 In distribution
UHSL6 In distribution
UHSOV In distribution
UHSM6 In distribution
UMS3 Withdrawn
UMM3 Withdrawn
UMR3 Withdrawn
UML1 Withdrawn

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
DynaMesh FEG Textiltechnik Forschungs- und Entwicklungsges. mbH 45
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