Data / Medical devices / China / Lifestyles Health Products Co., Ltd.
Lifestyles Health Products Co., Ltd.: FDA-registered device maker in Xianning Hubei, China, 1 510(k) clearance
Lifestyles Health Products Co., Ltd. is registered with the FDA (registration 3033840300) in Xianning Hubei, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 18, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3033840300
- Address
- 39 Guishan Road, Xianning High-tech Industrial Development Zone, Xianning Hubei, China, 437035
- Owner or operator
- LifeStyles Health Products Co., Ltd. (10091630)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- October 20, 2024
- Registered through
- 2026
- Brand names listed
- IPL Home Use Hair Removal Device, Model: D-T019, Jissbon silicone lubricant, Jissbon water-based lubricant, Jissbon toy lubricant,Jissbon warming lubricant,Jissbon strawberry flavored lubricant
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Exporter to the US | accessdata.fda.gov |
| Lubricant, Patient | KMJ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 18, 2024 | K240583 | IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W) | OHT | Substantially Equivalent | Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 18, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.