Arco Medic, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Arco Medic, Ltd. makes
Arco Medic, Ltd. manufactures the FLEXIBLADE, a surgical cutting instrument designed for precision tissue dissection in minimally invasive procedures.
The FLEXIBLADE is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Flexiblade Ref K984101
Regimes: CE MDR 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arco Medic, Ltd. have in the registry?
The registry currently lists 1 device for Arco Medic, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arco Medic, Ltd.'s devices?
Among its 1 most recently registered device, Arco Medic, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Arco Medic, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Arco Medic, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arco Medic, Ltd. in the registry?
The most recently registered devices listed for Arco Medic, Ltd. include FLEXIBLADE.