Allonus Tech Co., Ltd.
South KoreaFDA applicant, unverified FDA FEI 3035532393
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Allonus Tech Co., Ltd. makes
Allonus Tech Co., Ltd. designs and manufactures prosthetic devices tailored for limb replacement, focusing on functional and durable solutions for amputees.
The company’s prosthetic products fall under FDA Class II devices and are registered via the 510(k) pathway. Allonus Tech Co., Ltd. is based in the United States.
Catalogue
ALLONUS Tech Prosthetics Ref K241616
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3035532393
- Address
- 23-3, Sanmakgongdannam 4-gil, Yangsan-si Gyeongnam
Frequently asked questions
How many devices does Allonus Tech Co., Ltd. have in the registry?
The registry currently lists 1 device for Allonus Tech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allonus Tech Co., Ltd.'s devices?
Among its 1 most recently registered device, Allonus Tech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Allonus Tech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Allonus Tech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Allonus Tech Co., Ltd. in the registry?
The most recently registered devices listed for Allonus Tech Co., Ltd. include ALLONUS Tech Prosthetics.