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Composix 0123114

by Davol Inc.

Composix 0123114 is a Class II device made by Davol Inc., listed in FDA GUDID since 19 Aug 2015 (UDI-DI 00801741031175), 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 Number00801741031175 UDI-DI Date19 Aug 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  • Withdrawn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
Composix
Generic name
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
Model / Ref / Catalog
0123114
Primary DI / UDI-DI
00801741031175
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
Width — 35.6 Centimeter
Length — 25.4 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)