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 its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Gebr. Brasseler GmbH & Co. KG and its 1 subsidiaries with 2 510(k) clearances and 1 device recall. The most recent is a device recall dated Jan 28, 2022: Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Gebr. Brasseler GmbH & Co. KG and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 28, 2022 | Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35SClass II · One lot of product was distributed in unsealed packaging | Device recalls |
| Jul 26, 2013 | KOMET MEDICAL KIRSCHNER WIRES, STEINMANN PINS AND GUIDE PINS AND SCREWSK131264 · HWC | 510(k) clearances |
| Jun 29, 2007 | CERADRILLK071352 · EJL | 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
