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Ventralight 5955810

by Davol Inc.

Ventralight 5955810 is a Class II device made by Davol Inc., listed in FDA GUDID since 18 May 2015 (UDI-DI 00801741031786), 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 Number00801741031786 UDI-DI Date18 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  • Withdrawn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
5955810
Primary DI / UDI-DI
00801741031786
FDA product code
FTL, GCJ, OQL
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 — 20.3 Centimeter
Length — 25.4 Centimeter

Related devices

Category: Extra-gynaecological surgical mesh, composite-polymerSurgical mesh laparoscopic delivery/positioning device

Similar devices

Other devices filed under FDA product code FTL (Mesh, surgical, polymeric).

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)