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Ventralight 5991520

by Davol Inc.

Ventralight 5991520 is a Class II device made by Davol Inc., listed in FDA GUDID since 25 Aug 2017 (UDI-DI 00801741131004), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741131004 UDI-DI Date25 Aug 2017ListedStatusListed 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  • Withdrawn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
Surgical mesh laparoscopic delivery/positioning device
Model / Ref / Catalog
5991520
Primary DI / UDI-DI
00801741131004
FDA product code
ORQ, GCJ, FTL
GMDN term
Surgical mesh laparoscopic delivery/positioning device
Device class
Class II
Regulation number
878.3300, 876.1500
GUDID distribution status
In Commercial Distribution
Size
Length — 20 Centimeter
Width — 15 Centimeter

Related devices

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

Similar devices

Other devices filed under FDA product code GCJ.

Other devices from Davol Inc.

See all devices from Davol Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)