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OsteoMed 299-9208

by Osteomed Corp.

OsteoMed 299-9208 is a Class II device made by Osteomed Corp., listed in FDA GUDID since 8 Nov 2019 (UDI-DI 00842528110935), 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 Number00842528110935 UDI-DI Date8 Nov 2019ListedStatusListed 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  • Withdrawn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 bone screw, non-bioabsorbable, non-sterile
Model / Ref / Catalog
299-9208
Primary DI / UDI-DI
00842528110935
FDA product code
KCT
GMDN term
Craniofacial bone screw, non-bioabsorbable, non-sterile
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 8 Millimeter

Related devices

Category: Craniofacial bone screw, non-bioabsorbable, non-sterile

Similar devices

Other devices filed under FDA product code KCT (Sterilization wrap containers, trays, cassettes & other accessories).

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)