Ventralight

Ventralight ST Mesh with Echo PS Positioning System, 8" x 10" (20.3 x 25.4 cm), Ellipse

Registry build 21.09.26
1manufacturer
16catalogue numbers in this listing
4510(k) clearances naming this product code

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 Ventralight
Listed by Davol Inc., United States
FDA product code FTL
Device type Mesh, Surgical, Polymeric
Device class Class 2
Regulation 21 CFR 878.3300
Establishment Manufacturer
Record published 2017-08-25
Record revised 2024-10-22 (version 6)

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, manufacturing date
Storage Storage environment temperature 2 to 25 °C
Sizes Length 15 to 35.6 cm; width 10 to 30.5 cm; outer diameter 11.4 to 20.3 cm

Catalogue Numbers

Catalogue numbers for Ventralight
Catalogue number Size Status
5991015 Length 15 cm In distribution
5990015 Outer Diameter 15 cm In distribution
5954800 Outer Diameter 20.3 cm In distribution
5954790 Length 22.9 cm In distribution
5954810 Length 25.4 cm In distribution
5954460 Length 15.2 cm In distribution
5954124 Width 30.5 cm In distribution
5955810 Width 20.3 cm In distribution
5954600 Outer Diameter 15.2 cm In distribution
5954610 Length 25.4 cm In distribution
5993035 Width 30 cm In distribution
5954113 Length 33.0 cm In distribution
5954680 Length 20.3 cm In distribution
5955450 Diameter = 11.4 centimetre (cm) In distribution
5955610 Width 15.2 cm In distribution
5954450 Outer Diameter 11.4 cm 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
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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251557 2025-06-12
K250098 2025-04-09
K003323 2001-01-22
K792281 1979-11-27

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