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 Geister Medizin Technik with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 6, 2025: Geister K-Rex rongeurs.
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.
| Jun 6, 2025 | Geister K-Rex rongeursK242759 · HAE | 510(k) clearances |
| Aug 29, 2018 | Geister retractor for neuro - and spine surgeryK180610 · GZT | 510(k) clearances |
| Jul 1, 2004 | VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-7520K022823 · MGZ | 510(k) clearances |
| Jul 12, 2003 | KAMAR ANNULUS DILATOR + SIZER; GARRETT, COOLEY, AND DEBAKEY VESSEL DILATORSK030788 · DWP | 510(k) clearances |
| Apr 8, 1999 | ATRAUMATIC VASCULAR CLAMPS, MODEL #'S 22-XXXX, 23-XXXX, 03-60XX, 25-XXXX MICRO VASCULAR CLAMPS MODEL # 75-0XXX, ATRAUMATK982365 · DXC | 510(k) clearances |
| Jan 27, 1994 | GEISTER SURGICAL INT'L BIPOLAR ENDOSCOPIC SURGICAL INSTRUMENTSK933699 · GEI | 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
