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OsteoMed 212-1683

by Osteomed Corp.

OsteoMed 212-1683 is a Class II device made by Osteomed Corp., listed in FDA GUDID since 23 Jun 2015 (UDI-DI 00845694060875), 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 Number00845694060875 UDI-DI Date23 Jun 2015ListedStatusListed 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  • Withdrawn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
OsteoMed
Generic name
Craniofacial fixation plate kit, non-bioabsorbable
Model / Ref / Catalog
212-1683
Primary DI / UDI-DI
00845694060875
FDA product code
JEY
GMDN term
Craniofacial fixation plate kit, non-bioabsorbable
Device class
Class II
Regulation number
872.4760
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Craniofacial fixation plate kit, non-bioabsorbable

Similar devices

Other devices filed under FDA product code JEY (PLATE, BONE).

Other devices from Osteomed Corp.

See all devices from Osteomed Corp. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)