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OsteoMed 214-0083-SP-02

by Osteomed Corp.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845694064392 UDI-DI Date30 Jun 2015ListedStatusListed 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  • Withdrawn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
OsteoMed
Generic Name
Craniofacial fixation plate, non-bioabsorbable, non-customized
Model / Ref / Catalog
214-0083-SP-02
Primary DI / UDI-DI
00845694064392
FDA Product Code
DZL
GMDN Term
Craniofacial fixation plate, non-bioabsorbable, non-customized
Device Class
Class II
Regulation Number
872.4880
GUDID distribution status
In Commercial Distribution
Size
Length — 39 Millimeter

Related devices

Category: Craniofacial fixation plate, non-bioabsorbable, non-customized

Other devices from Osteomed Corp.

See all devices from Osteomed Corp. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No