Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Creo Medical, Ltd.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories3
Latest FDA decision2025-06-06
TypeNumberDevice NameCodeDateActions
510(k) K242774 SpydrBlade Flex Instrument (PRD-RG1-001)KNS2025-06-06 View
510(k) K242983 CROMA Electrosurgical Generator (PRD-EMR-050)GEI2025-02-05 View
510(k) K242061 Reusable Interface Cable 1.5 m (PRD-IFC-002)KNS2024-08-15 View
510(k) K230328 Speedboat Flush SB1 InstrumentKNS2023-10-31 View
510(k) K223138 AB1 Electrosurgical Instrument, Creo Electrosurgical SystemNEY2023-06-26 View
510(k) K221672 Creo Electrosurgical System with NP1 InstrumentNEY2023-02-14 View
510(k) K200298 ABI Instrument, Creo Electrosurgical SystemNEY2021-01-05 View
510(k) K200003 NP1 Instrument, Creo Electrosurgical SystemNEY2020-10-28 View
510(k) K192905 Creo Electrosurgical System with HS1 Hemostasis AccessoryKNS2020-03-19 View
510(k) K171983 Creo Medical Electrosurgical System including Speedboat RS2 Surgical AccessoryKNS2017-08-17 View

Related Clinical Trials