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Ambler Surgical Stevens tenotomy scissors

by Ambler Surgical, LLC 60 variants

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 Number00190660170738 UDI-DI Date7 Jan 2021ListedStatusListed 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  • Withdrawn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
Ambler Surgical
Generic Name
General-purpose surgical scissors, reusable
Model / Ref / Catalog
Stevens tenotomy scissors, 80-202
Primary DI / UDI-DI
00190660170738
FDA Product Code
HNF
GMDN Term
General-purpose surgical scissors, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: General-purpose surgical scissors, reusable

Other devices from Ambler Surgical, LLC

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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