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Bone Grinder 355-265

by Sontec Instruments, Inc.

Bone Grinder 355-265 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 17 Sep 2018 (UDI-DI 00192896032613), 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 Number00192896032613 UDI-DI Date17 Sep 2018ListedStatusListed 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  • Withdrawn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
Bone Grinder
Generic name
Manual bone mill
Model / Ref / Catalog
355-265
Primary DI / UDI-DI
00192896032613
FDA product code
LYS
GMDN term
Manual bone mill
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual bone mill

Similar devices in this category

Other devices filed under Manual bone mill.

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

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