Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Biedermann Motech with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 20, 2021: MOSS VRS Spinal System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 20, 2021 | MOSS VRS Spinal SystemK203607 · NKB | 510(k) clearances |
| Sep 13, 2018 | MOSS VRS Spinal SystemK181821 · NKB | 510(k) clearances |
| Jun 2, 2017 | TELIX K Interbody SystemK170890 · MAX | 510(k) clearances |
| Nov 17, 2016 | MOSS 100 Pedicle Screw SystemK162232 · NKB | 510(k) clearances |
| Apr 25, 1990 | BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEMK894184 · JDN | 510(k) clearances |
| Mar 20, 1990 | MOTECH TITANIUM SURGICAL MESHK900138 · EZX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
