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 Guenter Bissinger Medizintechnik GmbH with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 17, 2022: Supra Non-Stick Bipolar Forceps.
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.
| Nov 17, 2022 | Supra Non-Stick Bipolar ForcepsK213042 · GEI | 510(k) clearances |
| Feb 20, 2015 | Bissinger Monopolar CablesK150024 · GEI | 510(k) clearances |
| Jul 29, 2005 | CLARIS NON-STICK BIPOLAR FORCEPSK051429 · GEI | 510(k) clearances |
| Oct 27, 2004 | BITECH BIPOLAR SCISSORSK042077 · GEI | 510(k) clearances |
| Aug 6, 1998 | BISSINGER CABLES, CAT. NO. 801000XXK981919 · GEI | 510(k) clearances |
| May 21, 1998 | BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPSK970968 · HET | 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
