KARL STORZ Endoscopy-America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
KARL STORZ Endoscopy-America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: KARL STORZ Laryngoscopes and Accessories, KARL STORZ Holders, HOPKINS Telescopes
362
Total
362
Cleared
0
Denied
KARL STORZ Endoscopy-America, Inc. has 362 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Latest FDA clearance: May 2026. Active since 1980.
Browse the FDA 510(k) cleared devices submitted by KARL STORZ Endoscopy-America, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Karl Storz Endoscopy America, Inc., Karl Storz-Endoscopy-America, Inc. and Toscano Consulting.
FDA 510(k) Regulatory Record - KARL STORZ Endoscopy-America, Inc.
362 devices
Cleared
May 15, 2026
KARL STORZ Laryngoscopes and Accessories
Ear, Nose, Throat
270d
Cleared
Oct 22, 2024
KARL STORZ Holders
General & Plastic Surgery
244d
Cleared
Sep 14, 2023
HOPKINS Telescopes
Obstetrics & Gynecology
261d
Cleared
Jun 23, 2023
KOH Ultramicro Injection Cannula (26167NN)
General & Plastic Surgery
133d
Cleared
Apr 27, 2023
UNIDRIVE SIII System
Obstetrics & Gynecology
155d
Cleared
Mar 30, 2023
HOPKINS Telescopes
General & Plastic Surgery
90d
Cleared
Mar 17, 2023
KARL STORZ Bipolar Resectoscopes with HF Cable
Gastroenterology & Urology
261d
Cleared
Dec 20, 2022
HOPKINS Telescopes
General & Plastic Surgery
259d
Cleared
Nov 10, 2022
H1
General & Plastic Surgery
84d
Cleared
Jun 23, 2022
HD Mediastinoscope
Ear, Nose, Throat
267d
Cleared
May 13, 2022
Telepack +
Gastroenterology & Urology
18d
Cleared
Sep 03, 2021
KARL STORZ Flexible HD Cysto-Urethroscope System
Gastroenterology & Urology
28d
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