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Caspar Distractor Vertebral Retractor 416-305

by Sontec Instruments, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896037212 UDI-DIDate17 Sep 2018ListedStatusListed 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  • Withdrawn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 23 Oct 2026.

Specification

GUDID

Trade Name
Caspar Distractor Vertebral Retractor
Generic Name
Surgical retractor/retraction system blade, reusable
Model / Ref / Catalog
416-305
Primary DI / UDI-DI
00192896037212
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

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