ClearanceBrief
Company ยท GB

Creo Medical, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2025. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)5
NEYSystem, Ablation, Microwave And Accessories4
GEIElectrosurgical, Cutting & Coagulation & Accessories1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 6, 2025K242774SpydrBlade Flex Instrument (PRD-RG1-001)
Creo Medical, Ltd., GB
KNS
Feb 5, 2025K242983CROMA Electrosurgical Generator (PRD-EMR-050)
Creo Medical, Ltd., GB
GEI
Aug 15, 2024K242061Reusable Interface Cable 1.5 m (PRD-IFC-002)
Creo Medical, Ltd., GB
KNS
Oct 31, 2023K230328Speedboat Flush SB1 Instrument
Creo Medical, Ltd., GB
KNS
Jun 26, 2023K223138AB1 Electrosurgical Instrument, Creo Electrosurgical System
Creo Medical, Ltd., UA
NEY
Feb 14, 2023K221672Creo Electrosurgical System with NP1 Instrument
Creo Medical, Ltd., GB
NEY
Jan 5, 2021K200298ABI Instrument, Creo Electrosurgical System
Creo Medical, Ltd., GB
NEY
Oct 28, 2020K200003NP1 Instrument, Creo Electrosurgical System
Creo Medical, Ltd., GB
NEY
Mar 19, 2020K192905Creo Electrosurgical System with HS1 Hemostasis Accessory
Creo Medical, Ltd., GB
KNS
Aug 17, 2017K171983Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory
Creo Medical, Ltd., GB
KNS

Latest recalls

DateFirm and productCodeLinked 510(k)
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