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Sterile Hook/Triangle Blade Pack for Endotrac Endoscopic Carpal Tunnel Release 2056

by Restore Surgical LLC GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10815375022185 UDI-DIDate23 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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 23 Oct 2026.

Specification

GUDID

Trade Name
Sterile Hook/Triangle Blade Pack for Endotrac Endoscopic Carpal Tunnel Release
Generic Name
Manual scalpel blade, single-use
Model / Reference
2056
Primary DI / UDI-DI
10815375022185
FDA Product Code
HRX
GMDN Term
Manual scalpel blade, single-use
Device Class
Class II
Regulation Number
888.1100
GUDID distribution status
Not in Commercial Distribution

Other devices from Restore Surgical LLC

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No