510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K242759Substantially Equivalent

Geister K-Rex rongeurs

Geister Medizin Technik GmbH, Tuttlingen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K242759 is the FDA 510(k) clearance record for Geister K-Rex rongeurs, a class II device, cleared for Geister Medizin Technik GmbH on under FDA product code HAE (Rongeur, Manual). FDA records list 6 510(k) clearances for Geister Medizin Technik GmbH, from to . As of , FDA records show no recalls naming K242759.

Clearance record

Decision date
Received
(267 days to decision)
Product code
HAE Rongeur, Manual
Regulation
21 CFR 882.4840
Device class
Class II
Review panel
Neurology
Applicant
Geister Medizin Technik GmbH Foehrenstrasse 2, Tuttlingen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HAE

Trailing 12 months
1 clearance under product code HAE in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HAE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260