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Optifix 0113330

by Davol Inc.

Optifix 0113330 is a Class II device made by Davol Inc., listed in FDA GUDID since 18 Jul 2019 (UDI-DI 00801741136566), 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 Number00801741136566 UDI-DI Date18 Jul 2019ListedStatusListed 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  • Withdrawn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
Optifix
Generic name
Soft-tissue/mesh anchor, bioabsorbable
Model / Ref / Catalog
0113330
Primary DI / UDI-DI
00801741136566
FDA product code
GDW
GMDN term
Soft-tissue/mesh anchor, bioabsorbable
Device class
Class II
Regulation number
878.4750
GUDID distribution status
In Commercial Distribution
Size
Length — 37 Centimeter
Outer Diameter — 5 Millimeter

Related devices

Category: Soft-tissue/mesh anchor, bioabsorbable

Similar devices

Other devices filed under FDA product code GDW (Staple, implantable).

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)