Karl Storz SE & CO. KG
US Last updated 23 May 2026
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- Devices
- 9,095
- Registries
- FDA 510(k)GUDIDEUDAMED
- FDA recalls
- 0
Catalogue
Karl Storz Supraloop Ref K254303
n.a. 791003DS Ref 791003DS
n.a. 268015 Ref 268015
n.a. 744101 Ref 744101
n.a. 28163ZSH Ref 28163ZSH
n.a. 11603ZS Ref 11603ZS
n.a. 770003 Ref 770003
n.a. 498613 Ref 498613
n.a. 204015 Ref 204015
n.a. 8594D Ref 8594D
SilCut 28171SBN Ref 28171SBN
n.a. 10040AA Ref 10040AA
n.a. 8681D Ref 8681D
n.a. 41201KN Ref 41201KN
n.a. 28164MRA Ref 28164MRA
Vaporcut 27043WG Ref 27043WG
n.a. 8593AM Ref 8593AM
n.a. 11005EK Ref 11005EK
n.a. 8603KA Ref 8603KA
n.a. 403950 Ref 403950
SilCut 28171KUN Ref 28171KUN
Easygo! 28163GTZ Ref 28163GTZ
n.a. 8660W Ref 8660W
n.a. 123035 Ref 123035
n.a. 403865 Ref 403865
n.a. 653010 Ref 653010
Take-Apart 26176HV Ref 26176HV
n.a. 26167KFS Ref 26167KFS
n.a. 40800083 Ref 40800083
n.a. 28163CSS Ref 28163CSS
Take-Apart 26176HT Ref 26176HT
n.a. 10510CA Ref 10510CA
n.a. 629704 Ref 629704
Clickline 33300 Ref 33300
n.a. 224600 Ref 224600
n.a. 13273SC Ref 13273SC
n.a. 8541D Ref 8541D
n.a. 479800 Ref 479800
n.a. 10357P Ref 10357P
n.a. 403835 Ref 403835
Clickline 30133 Ref 30133
n.a. 28163MN Ref 28163MN
n.a. 649635HK Ref 649635HK
n.a. 58126 Ref 58126
n.a. 20016831 Ref 20016831
n.a. 27050NP-S Ref 27050NP-S
n.a. 495VIT Ref 495VIT
n.a. 723540A Ref 723540A
n.a. 26169KK Ref 26169KK
n.a. 225008 Ref 225008
Showing 1-50 of 9,095
What Karl Storz SE & CO. KG makes
The company manufactures surgical and diagnostic devices for minimally invasive procedures, including trocars with valve seals for laparoscopic access, laser accessories for urological applications, and flexible endoscopes for intubation, cystoscopy, and ureterorenoscopy. Their portfolio also covers pediatric cysto-urethro fiberscopes, video rhino-laryngoscopes, cholangiography sets, and nephroscopy systems for kidney stone management. Additional products include insufflation devices (e.g., ENDOFLATOR +) and fiber telescopes for urological imaging.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company’s products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Information
- Country
- US