MANTIZ Co., Ltd.
Country not established FDA establishment FEI 3021389253
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
QUATTRO Spinal system (Open Configuration) Ref K260362
510(k) 510(k)
Company details
- FDA FEI number
- 3021389253
- Address
- 423-15, Hyeoksin-daero, Dong-gu, Daegu
Frequently asked questions
How many devices does MANTIZ Co.,Ltd. have in the registry?
The registry currently lists 1 device for MANTIZ Co.,Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MANTIZ Co.,Ltd.'s devices?
Among its 1 most recently registered device, MANTIZ Co.,Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do MANTIZ Co.,Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for MANTIZ Co.,Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MANTIZ Co.,Ltd. in the registry?
The most recently registered devices listed for MANTIZ Co.,Ltd. include QUATTRO Spinal system (Open Configuration).