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OsteoMed 323-1240-SP-02

by Osteomed Corp.

OsteoMed 323-1240-SP-02 is a Class II device made by Osteomed Corp., listed in FDA GUDID since 21 Jul 2016 (UDI-DI 00845694076524), 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 Number00845694076524 UDI-DI Date21 Jul 2016ListedStatusListed 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  • Withdrawn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
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
323-1240-SP-02
Primary DI / UDI-DI
00845694076524
FDA product code
HRS
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 4 Millimeter

Related devices

Category: General internal orthopaedic fixation system implantation kit

Similar devices in this category

Other devices filed under General internal orthopaedic fixation system implantation kit.

Other devices from Osteomed Corp.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)