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Life Instruments 810-0700-0

by Life Instrument Corporation

Life Instruments 810-0700-0 is a Class I device made by Life Instrument Corporation, listed in FDA GUDID since 12 Feb 2021 (UDI-DI M930810070000), 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 NumberM930810070000 UDI-DI Date12 Feb 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  • Withdrawn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
Life Instruments
Generic name
Bone curette, reusable
Model / reference
810-0700-0
Primary DI / UDI-DI
M930810070000
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

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Properties

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