Serapis Medical Electronics, Co.
Country not established
- Devices
- 1
What Serapis Medical Electronics, Co. makes
Serapis Medical Electronics manufactures the TUFCOTE Epilation Probe, a device designed for laser hair removal procedures. This probe is intended to assist in the precise application of laser energy to target hair follicles during epilation treatments.
The TUFCOTE Epilation Probe is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Tufcote Epilation Probe Ref K831048
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Serapis Medical Electronics, Co. have in the registry?
The registry currently lists 1 device for Serapis Medical Electronics, Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Serapis Medical Electronics, Co.'s devices?
Among its 1 most recently registered device, Serapis Medical Electronics, Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Serapis Medical Electronics, Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Serapis Medical Electronics, Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Serapis Medical Electronics, Co. in the registry?
The most recently registered devices listed for Serapis Medical Electronics, Co. include TUFCOTE EPILATION PROBE.