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X-Pac EI3016

by Expanding Innovations, Inc.

X-Pac EI3016 is a Class I device made by Expanding Innovations, Inc., listed in FDA GUDID since 26 May 2023 (UDI-DI 00850001720588), 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 Number00850001720588 UDI-DI Date26 May 2023ListedStatusListed 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  • Withdrawn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
X-Pac
Generic name
Orthopaedic implantation hammering attachment
Model / reference
EI3016
Primary DI / UDI-DI
00850001720588
FDA product code
LXH
GMDN term
Orthopaedic implantation hammering attachment
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 implantation hammering attachment

Other devices from Expanding Innovations, Inc.

See all devices from Expanding Innovations, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)