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BOSS Instruments 65-6290

by Boss Instruments, Ltd.

BOSS Instruments 65-6290 is a Class II device made by Boss Instruments, Ltd., listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00888515110649), 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 Number00888515110649 UDI-DI Date21 Sep 2016ListedStatusListed 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  • Withdrawn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, scissors-like, reusable
Model / Ref / Catalog
65-6290
Primary DI / UDI-DI
00888515110649
FDA product code
DXC
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class II
Regulation number
870.4450
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Similar devices in this category

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

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)