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Bone Chisel Chandler 10-5311HD

by W.H. Holden, Inc.

Bone Chisel Chandler 10-5311HD is a Class I device made by W.H. Holden, Inc., listed in FDA GUDID since 10 Oct 2023 (UDI-DI D928105311HD0), 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 NumberD928105311HD0 UDI-DI Date10 Oct 2023ListedStatusListed 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  • Withdrawn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
Bone Chisel Chandler
Generic name
Nasal chisel
Model / reference
10-5311HD
Primary DI / UDI-DI
D928105311HD0
FDA product code
EMM
GMDN term
Nasal chisel
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Nasal chisel

Similar devices in this category

Other devices filed under Nasal chisel.

Other devices from W.H. Holden, Inc.

See all devices from W.H. Holden, Inc. →

Properties

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