Ace Medical Industry Co., Ltd.
South KoreaFDA applicant, unverified FDA FEI 3019012929
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Ace Medical Industry Co., Ltd. makes
Ace Medical Industry Co., Ltd. manufactures the ACE Cannula, a medical device designed for specific procedural applications in clinical settings.
The ACE Cannula is classified as a Class II device under FDA regulations and is listed in the 510(k) registry. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
ACE Cannula Ref K242741
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019012929
- DUNS number
- 688454651
- Address
- 57-14 , Gwangjeok ro 228beon gil, Gwang jeok myeon, Yangju-si Gyeonggi
- [email protected]
- Phone
- +821075194237
Frequently asked questions
How many devices does Ace Medical Industry Co., Ltd. have in the registry?
The registry currently lists 3 devices for Ace Medical Industry Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ace Medical Industry Co., Ltd.'s devices?
Among its 3 most recently registered devices, Ace Medical Industry Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ace Medical Industry Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ace Medical Industry Co., Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ace Medical Industry Co., Ltd. in the registry?
The most recently registered devices listed for Ace Medical Industry Co., Ltd. include ACE CANNULA B-18100, ACE MESO THERAPIE SN-3204 and ACE Cannula.