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Osteomed 336-3530-T

by Osteomed Corp.

Osteomed 336-3530-T is a Class II device made by Osteomed Corp., listed in FDA GUDID since 15 Sep 2026 (UDI-DI 00845694044097), 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 Number00845694044097 UDI-DI Date15 Sep 2026ListedStatusListed 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  • Withdrawn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
Surgical implant template, reusable
Model / reference
336-3530-T
Primary DI / UDI-DI
00845694044097
FDA product code
JEY
GMDN term
Surgical implant template, reusable
Device class
Class II
Regulation number
872.4760
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code JEY (PLATE, BONE).

Other devices from Osteomed Corp.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)