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BOSS Instruments 95-9175

by Boss Instruments, Ltd.

BOSS Instruments 95-9175 is a Class I device made by Boss Instruments, Ltd., listed in FDA GUDID since 29 Feb 2024 (UDI-DI 00888515249202), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888515249202 UDI-DI Date29 Feb 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
BOSS Instruments
Generic name
Surgical soft-tissue manipulation forceps, alligator, reusable
Model / Ref / Catalog
95-9175
Primary DI / UDI-DI
00888515249202
FDA product code
KAE
GMDN term
Surgical soft-tissue manipulation forceps, alligator, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical soft-tissue manipulation forceps, alligator, reusable

Similar devices in this category

Other devices filed under Surgical soft-tissue manipulation forceps, alligator, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)