Skip to content

Upper Extremity, Ips 60-011-68-09-LP

by KLS-Martin L.P.

Upper Extremity, Ips 60-011-68-09-LP is a Class II device made by KLS-Martin L.P., listed in FDA GUDID since 21 Oct 2026 (UDI-DI 00888118155702), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888118155702 UDI-DI Date21 Oct 2026ListedStatusListed 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  • Withdrawn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
Upper Extremity, Ips
Generic name
Custom-made organ/bone anatomy model/surgical guide kit
Model / reference
60-011-68-09-LP
Primary DI / UDI-DI
00888118155702
FDA product code
PBF, HRS
GMDN term
Custom-made organ/bone anatomy model/surgical guide kit
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from KLS-Martin L.P.

See all devices from KLS-Martin L.P. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)