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Kugel 0115812

by Davol Inc.

Kugel 0115812 is a Class II device made by Davol Inc., listed in FDA GUDID since 17 May 2015 (UDI-DI 00801741030802), 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 Number00801741030802 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  • Withdrawn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
Kugel
Generic name
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
Model / Ref / Catalog
0115812
Primary DI / UDI-DI
00801741030802
FDA product code
FTL
GMDN term
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 11.4 Centimeter

Related devices

Category: Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

Similar devices in this category

Other devices filed under Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable.

Other devices from Davol Inc.

See all devices from Davol Inc. →

Properties

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