Creo Medical, Ltd. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Creo Medical, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Chepstow, GB.
Latest FDA clearance: Jun 2025. Active since 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Creo Medical, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Creo Medical, Ltd.
10 devices
Cleared
Jun 06, 2025
SpydrBlade Flex Instrument (PRD-RG1-001)
Gastroenterology & Urology
266d
Cleared
Feb 05, 2025
CROMA Electrosurgical Generator (PRD-EMR-050)
General & Plastic Surgery
132d
Cleared
Aug 15, 2024
Reusable Interface Cable 1.5 m (PRD-IFC-002)
Gastroenterology & Urology
31d
Cleared
Oct 31, 2023
Speedboat Flush SB1 Instrument
Gastroenterology & Urology
267d
Cleared
Jun 26, 2023
AB1 Electrosurgical Instrument, Creo Electrosurgical System
General & Plastic Surgery
265d
Cleared
Feb 14, 2023
Creo Electrosurgical System with NP1 Instrument
General & Plastic Surgery
250d
Cleared
Jan 05, 2021
ABI Instrument, Creo Electrosurgical System
General & Plastic Surgery
334d
Cleared
Oct 28, 2020
NP1 Instrument, Creo Electrosurgical System
General & Plastic Surgery
300d
Cleared
Mar 19, 2020
Creo Electrosurgical System with HS1 Hemostasis Accessory
Gastroenterology & Urology
156d
Cleared
Aug 17, 2017
Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory
Gastroenterology & Urology
48d