Ventralight 5993035
by Davol Inc.
Ventralight 5993035 is a Class II device made by Davol Inc., listed in FDA GUDID since 25 Aug 2017 (UDI-DI 00801741131066), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00801741131066 | Date25 Aug 2017 | StatusListed |
Official records
- AccessGUDID record 00801741131066
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ventralight
- Generic name
- Extra-gynaecological surgical mesh, composite-polymer
- Model / Ref / Catalog
- 5993035
- Primary DI / UDI-DI
- 00801741131066
- FDA product code
- FTL, GCJ, ORQ
- GMDN term
- Extra-gynaecological surgical mesh, composite-polymer
- Device class
- Class II
- Regulation number
- 878.3300, 876.1500
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 30 CentimeterLength — 35 Centimeter
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