Skip to the page

Data / Medical devices / Plate, Fixation, Bone, Non-Spinal, Metallic

Plate, Fixation, Bone, Non-Spinal, Metallic (NDF): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Plate, Fixation, Bone, Non-Spinal, Metallic (product code NDF, Class 2, 21 CFR 888.3030). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on August 22, 2005, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
NDF
Device class
2
Regulation
888.3030
Medical specialty
Orthopedic
Implant
Yes

Makers by country

CountryMakers
China2
United States1
Austria1

Makers of Plate, Fixation, Bone, Non-Spinal, Metallic

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biomet, Inc.Warsaw, IN, United StatesManufacturer2August 12, 2002000api.fda.gov
Zhejiang Biomet Medical Products Co., Ltd.Jinhua Zhejiang, ChinaManufacturer2August 12, 2002000api.fda.gov
I.T.S. GMBHLASSNITZHOEHE Steiermark, AustriaManufacturer1August 22, 2005000api.fda.gov
LX Precision Shanghai Co LtdShanghai, ChinaContract manufacturer0000api.fda.gov

Updated August 22, 2005. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.