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BoneScalpel BCM-HP

by Misonix, LLC

BoneScalpel BCM-HP is a device classified as Unclassified made by Misonix, LLC, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00841626100688), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841626100688 UDI-DI Date24 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  • Withdrawn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
BoneScalpel
Generic name
Hard-tissue ultrasonic surgical system handpiece
Model / reference
BCM-HP
Primary DI / UDI-DI
00841626100688
FDA product code
LFL
GMDN term
Hard-tissue ultrasonic surgical system handpiece
Device class
U
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Hard-tissue ultrasonic surgical system handpiece

Similar devices

Other devices filed under FDA product code LFL (Instrument, Ultrasonic Surgical).

Other devices from Misonix, LLC

See all devices from Misonix, LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)