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BoneScalpel MXB-10

by Misonix, LLC

BoneScalpel MXB-10 is a device classified as Unclassified made by Misonix, LLC, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00841626101104), 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 Number00841626101104 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  • Withdrawn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
Soft-tissue ultrasonic surgical system handpiece tip, single-use
Model / reference
MXB-10
Primary DI / UDI-DI
00841626101104
FDA product code
LFL
GMDN term
Soft-tissue ultrasonic surgical system handpiece tip, single-use
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Soft-tissue ultrasonic surgical system handpiece tip, single-use

Similar devices in this category

Other devices filed under Soft-tissue ultrasonic surgical system handpiece tip, single-use.

Other devices from Misonix, LLC

See all devices from Misonix, LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)