Karl Storz Knives, Curetts, Hooks, Probes

K945891 is the FDA 510(k) clearance record for KARL STORZ KNIVES, CURETTS, HOOKS, PROBES, a class II device, cleared for KARL STORZ Endoscopy-America, Inc. on 1995-06-09 under FDA product code HRX (Arthroscope). FDA's definition for product code HRX reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 402 510(k) clearances for KARL STORZ Endoscopy-America, Inc., from 1980-04-21 to 2026-05-15. As of 2026-09-10, FDA records show no recalls naming K945891.