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Ventralight 5954113

by Davol Inc.

Ventralight 5954113 is a Class II device made by Davol Inc., listed in FDA GUDID since 17 May 2015 (UDI-DI 00801741031595), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741031595 UDI-DI Date17 May 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Ventralight
Generic name
Extra-gynaecological surgical mesh, composite-polymer
Model / Ref / Catalog
5954113
Primary DI / UDI-DI
00801741031595
FDA product code
FTL
GMDN term
Extra-gynaecological surgical mesh, composite-polymer
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
Size
Length — 33.0 Centimeter
Width — 25.4 Centimeter

Related devices

Category: Extra-gynaecological surgical mesh, composite-polymer

Similar devices in this category

Other devices filed under Extra-gynaecological surgical mesh, composite-polymer.

Other devices from Davol Inc.

See all devices from Davol Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)