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Peri-Loc E0015158-1

by Smith & Nephew, Inc.

Peri-Loc E0015158-1 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 5 Aug 2016 (UDI-DI 00885556657386), 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 Number00885556657386 UDI-DI Date5 Aug 2016ListedStatusListed 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  • Withdrawn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
Peri-Loc
Generic name
Implant handling forceps, scissors-like
Model / Ref / Catalog
E0015158-1
Description
BALL SPIKE / PADDLE PELVIC REDUCTION FORCEPS
Primary DI / UDI-DI
00885556657386
FDA product code
LXH
GMDN term
Implant handling forceps, scissors-like
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Implant handling forceps, scissors-like

Similar devices

Other devices filed under FDA product code LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)