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OsteoMed 220-0640-86

by Osteomed Corp.

OsteoMed 220-0640-86 is a Class II device made by Osteomed Corp., listed in FDA GUDID since 22 Jul 2016 (UDI-DI 00845694059305), 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 Number00845694059305 UDI-DI Date22 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  • Withdrawn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
220-0640-86
Primary DI / UDI-DI
00845694059305
FDA product code
DZL
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class II
Regulation number
872.4880
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)