Alovea Healthcare Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3043105515
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Alovea Healthcare Co., Ltd. makes
Alovea Healthcare Co., Ltd. manufactures Intense Pulsed Light (IPL) hair removal devices designed for at-home use, including models like the I6 S1, I6 D1, and I6 M1. These devices target unwanted hair through controlled light energy to promote hair reduction.
The IPL hair removal devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
IPL Hair Removal Device (I6 S1, I6 D1, I6 M1) Ref K252618
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043105515
- DUNS number
- 450425100
- Address
- Room 703, Building 1, No. 188 Fu Chun Jiang Rd, New District, Suzhou Jiangsu
Frequently asked questions
How many devices does Alovea Healthcare Co. , Ltd. have in the registry?
The registry currently lists 4 devices for Alovea Healthcare Co. , Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alovea Healthcare Co. , Ltd.'s devices?
Among its 4 most recently registered devices, Alovea Healthcare 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 Alovea Healthcare Co. , Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Alovea Healthcare Co. , Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alovea Healthcare Co. , Ltd. in the registry?
The most recently registered devices listed for Alovea Healthcare Co. , Ltd. include carevia I6 S1, carevia I6 M1, carevia I6 D1 and IPL Hair Removal Device (I6 S1, I6 D1, I6 M1).