Biedermann Motech GmbH & Co. KG

FDA Regulatory Profile

Biedermann Motech GmbH & Co. KG has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 20, 2021

Reviewing Biedermann Motech GmbH & Co. KG as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Request a free FDA snapshot

Or get Biedermann Motech GmbH & Co. KG's full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K203607MOSS VRS Spinal SystemAug 20, 2021
K181821MOSS VRS Spinal SystemSep 13, 2018
K170890TELIX K Interbody SystemJun 2, 2017
K162232MOSS 100 Pedicle Screw SystemNov 17, 2016