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Agility 2555-32-030

by Depuy Orthopaedics, Inc.

Agility 2555-32-030 (255532030) is a Class I device made by Depuy Orthopaedics, Inc., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 10603295142362), 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 Number10603295142362 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
Agility
Generic name
Orthopaedic prosthesis implantation positioning instrument, single-use
Model / Ref / Catalog
2555-32-030, 255532030
Primary DI / UDI-DI
10603295142362
FDA product code
LXH
GMDN term
Orthopaedic prosthesis implantation positioning instrument, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic prosthesis implantation positioning instrument, single-use

Similar devices in this category

Other devices filed under Orthopaedic prosthesis implantation positioning instrument, single-use.

Other devices from Depuy Orthopaedics, Inc.

See all devices from Depuy Orthopaedics, Inc. →

Properties

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