ClearanceBrief
Company ยท DE

Geister Medizin Technik GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2025. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DWPDilator, Vessel, Surgical1
DXCClamp, Vascular1
GEIElectrosurgical, Cutting & Coagulation & Accessories1
GZTRetractor, Self-Retaining, For Neurosurgery1
HAERongeur, Manual1
MGZValvulotome1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 6, 2025K242759Geister K-Rex rongeurs
Geister Medizin Technik GmbH, DE
HAE
Aug 29, 2018K180610Geister retractor for neuro - and spine surgery
Geister Medizin Technik GmbH, DE
GZT
Jul 1, 2004K022823VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-7520
Geister Medizin Technik GmbH
MGZ
Jul 12, 2003K030788KAMAR ANNULUS DILATOR + SIZER; GARRETT, COOLEY, AND DEBAKEY VESSEL DILATORS
Geister Medizin Technik GmbH, NL
DWP
Apr 8, 1999K982365ATRAUMATIC VASCULAR CLAMPS, MODEL #'S 22-XXXX, 23-XXXX, 03-60XX, 25-XXXX MICRO VASCULAR CLAMPS MODEL # 75-0XXX, ATRAUMAT
Geister Medizin Technik GmbH, DE
DXC
Jan 27, 1994K933699GEISTER SURGICAL INT'L BIPOLAR ENDOSCOPIC SURGICAL INSTRUMENTS
Geister Medizin Technik GmbH
GEI

Latest recalls

DateFirm and productCodeLinked 510(k)
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