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Boss Instruments 70-0970

by Boss Instruments, Ltd.

Boss Instruments 70-0970 is a Class II device made by Boss Instruments, Ltd., listed in FDA GUDID since 1 Oct 2016 (UDI-DI 00888515137103), 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 Number00888515137103 UDI-DI Date1 Oct 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  • Withdrawn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
Spinal rongeur
Model / Ref / Catalog
70-0970
Primary DI / UDI-DI
00888515137103
FDA product code
HAE
GMDN term
Spinal rongeur
Device class
Class II
Regulation number
882.4840
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Spinal rongeur

Similar devices in this category

Other devices filed under Spinal rongeur.

Other devices from Boss Instruments, Ltd.

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Properties

  • Sterilise before use
  • Prescription use
Other properties (13, all answered No)