Flp Ent., Inc.
Country not established
- Devices
- 1
What Flp Ent., Inc. makes
Flp Ent., Inc. manufactures the LOKSHOT PISTON SYRINGE, a medical device designed for specific clinical applications.
The company's products are regulated as Class II devices and listed in the FDA 510(k) registry. Flp Ent., Inc. is based in the US.
Catalogue
Lokshot Piston Syringe Ref K891467
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flp Ent., Inc. have in the registry?
The registry currently lists 1 device for Flp Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flp Ent., Inc.'s devices?
Among its 1 most recently registered device, Flp Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Flp Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Flp Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flp Ent., Inc. in the registry?
The most recently registered devices listed for Flp Ent., Inc. include LOKSHOT PISTON SYRINGE.