OsteoMed 231-1051

by Osteomed Corp.

OsteoMed 231-1051 is a Class II device made by Osteomed Corp., listed in FDA GUDID since 2 Jul 2015 (UDI-DI 00845694056076), 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	Number00845694056076 UDI-DI	Date2 Jul 2015Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00845694056076

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: OsteoMed
Generic name: Craniofacial fixation plate, non-bioabsorbable, non-customized
Model / Ref / Catalog: 231-1051

Primary DI / UDI-DI: 00845694056076
FDA product code: JEY
GMDN term: Craniofacial fixation plate, non-bioabsorbable, non-customized

Device class: Class II
Regulation number: 872.4760
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Size: Length — 13 Millimeter

Similar devices in this category

Other devices filed under Craniofacial fixation plate, non-bioabsorbable, non-customized.

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Properties

Sterilise before use
Single use
Implantable
Prescription use
Lot / batch number
Manufacturing date

Other properties (9, all answered No)