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Ring Retractor Blade 516-967P

by Sontec Instruments, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896081017 UDI-DI Date20 Sep 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ring Retractor Blade
Generic Name
Surgical retractor/retraction system blade, reusable
Model / Ref / Catalog
516-967P
Primary DI / UDI-DI
00192896081017
FDA Product Code
FFO
GMDN Term
Surgical retractor/retraction system blade, reusable
Device Class
Class I
Regulation Number
876.4730
GUDID distribution status
In Commercial Distribution
Size
Width — 1.5 Inch
Length — 6 Inch

Related devices

Category: Surgical retractor/retraction system blade, reusable

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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