Creo Medical, Ltd.

Creo Medical, Ltd. holds 10 FDA 510(k) medical device clearances, first cleared 2017, most recent 2025.

Top product codes for Creo Medical, Ltd.

KNS — Gastroenterology, Urology5 devices
NEY — General, Plastic Surgery4 devices
GEI — General, Plastic Surgery1 device

Recent clearances by Creo Medical, Ltd.

K242774 — SpydrBlade Flex Instrument (PRD-RG1-001)Code KNS·2025-06-06
K242983 — CROMA Electrosurgical Generator (PRD-EMR-050)Code GEI·2025-02-05
K242061 — Reusable Interface Cable 1.5 m (PRD-IFC-002)Code KNS·2024-08-15
K230328 — Speedboat Flush SB1 InstrumentCode KNS·2023-10-31
K223138 — AB1 Electrosurgical Instrument, Creo Electrosurgical SystemCode NEY·2023-06-26
K221672 — Creo Electrosurgical System with NP1 InstrumentCode NEY·2023-02-14
K200298 — ABI Instrument, Creo Electrosurgical SystemCode NEY·2021-01-05
K200003 — NP1 Instrument, Creo Electrosurgical SystemCode NEY·2020-10-28
K192905 — Creo Electrosurgical System with HS1 Hemostasis AccessoryCode KNS·2020-03-19
K171983 — Creo Medical Electrosurgical System including Speedboat RS2 Surgical AccessoryCode KNS·2017-08-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.