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OsteoMed 308-3036-SP

by Osteomed Corp.

OsteoMed 308-3036-SP is a Class II device made by Osteomed Corp., listed in FDA GUDID since 24 Apr 2015 (UDI-DI 00845694035323), 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 Number00845694035323 UDI-DI Date24 Apr 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  • Withdrawn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
Orthopaedic bone screw, non-bioabsorbable, sterile
Model / Ref / Catalog
308-3036-SP
Primary DI / UDI-DI
00845694035323
FDA product code
HWC
GMDN term
Orthopaedic bone screw, non-bioabsorbable, sterile
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution
Size
Length — 36 Millimeter

Related devices

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Similar devices in this category

Other devices filed under Orthopaedic bone screw, non-bioabsorbable, sterile.

Other devices from Osteomed Corp.

See all devices from Osteomed Corp. →

Properties

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