Skip to content

BOSS Instruments 70-8752

by Boss Instruments, Ltd.

BOSS Instruments 70-8752 is a Class I device made by Boss Instruments, Ltd., listed in FDA GUDID since 29 Feb 2024 (UDI-DI 00888515167100), 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 Number00888515167100 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  • Withdrawn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
Bone curette, reusable
Model / Ref / Catalog
70-8752
Primary DI / UDI-DI
00888515167100
FDA product code
FZS
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusable

Similar devices in this category

Other devices filed under Bone curette, reusable.

Other devices from Boss Instruments, Ltd.

See all devices from Boss Instruments, Ltd. →

Properties

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