Skip to content

Tower ST Long Window 88974

by Premia Spine Ltd GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290115934076 UDI-DIDate1 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Tower ST Long Window
Generic Name
Orthopaedic implantation sleeve, reusable
Model / Reference
88974
Primary DI / UDI-DI
07290115934076
510(k) Number
FDA Product Code
NKB, MNI, MNH
GMDN Term
Orthopaedic implantation sleeve, reusable
Device Class
Class II
Regulation Number
888.3070
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Cleared under the same submission (K150380)

Show all (12)

Cleared under the same submission (K170061)

Show all (12)

Cleared under the same submission (K231844)

Show all (12)

Other devices from Premia Spine Ltd

See all devices from Premia Spine Ltd →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No