Idis Co., Ltd.
South KoreaFDA applicant, unverified FDA FEI 3026365523
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Idis Co., Ltd. makes
Idis Co., Ltd. manufactures the S-Plant Dental Implant System, a dental implant designed for osseointegration in the jawbone to support prosthetic teeth or dental restorations.
The S-Plant Dental Implant System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
S-Plant Dental Implant System Ref K231429
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3026365523
- DUNS number
- 695010523
- Address
- #1314 ~ #1319, 122, Jomaru-ro, 385 beon gil,, Bucheon-si Gyeonggi
Frequently asked questions
How many devices does Idis Co., Ltd. have in the registry?
The registry currently lists 4 devices for Idis Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Idis Co., Ltd.'s devices?
Among its 4 most recently registered devices, Idis Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Idis Co., Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Idis Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Idis Co., Ltd. in the registry?
The most recently registered devices listed for Idis Co., Ltd. include S-Plant SPFS7011W, S-Plant ISH705, S-Plant PISD6055H and S-Plant Dental Implant System.