03.815.029

03.815.029 (03815029) is a Class I device made by Synthes, listed in FDA GUDID since 30 Jun 2016 (UDI-DI 10705034728247), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10705034728247 UDI-DI	Date30 Jun 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10705034728247

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Bone distraction forceps
Model / Ref / Catalog: 03.815.029, 03815029

Primary DI / UDI-DI: 10705034728247
FDA product code: LXH
GMDN term: Bone distraction forceps

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)