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Integra® Miltex® 11672

by Integra LifeSciences Production Corporation

Integra® Miltex® 11672 (11-672) is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 15 Nov 2017 (UDI-DI 10381780354222), 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 Number10381780354222 UDI-DI Date15 Nov 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  • Withdrawn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
Integra® Miltex®
Generic name
Self-retaining surgical retractor, reusable
Model / Ref / Catalog
11672, 11-672
Primary DI / UDI-DI
10381780354222
FDA product code
GAD
GMDN term
Self-retaining surgical retractor, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Self-retaining surgical retractor, reusable

Similar devices in this category

Other devices filed under Self-retaining surgical retractor, reusable.

Other devices from Integra LifeSciences Production Corporation

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)