Data / Medical devices / China / Shenzhen Idea Light Limited
Shenzhen Idea Light Limited: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances
Shenzhen Idea Light Limited is registered with the FDA (registration 3015287734) in Shenzhen Guangdong, China. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 5, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3015287734
- Address
- 3rd Floor, Block B, Shengdelan Industry Park, Guanlan, Longhua District, Shenzhen Guangdong, China, 518110
- Owner or operator
- Shenzhen Idea Light Limited (10060135)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- April 3, 2019
- Registered through
- 2026
- Brand names listed
- Allevared (Model: LP-ALVRD-BLK); Allevared Pro (Model: LP-ALVRDP-BLK), Biocare (Model: LP-BCRE); BioHeal (Model: LP-BIOHL-BLK); BioHeal Plus (Model: LP-BIOHLPLS-BLK), CBG Medical LED Silicone Mask (model: TLM200, Erythros Laser Pro), Horizon (Model: RLPRO2000L-B); HS-TL2000L-B; IngraGlow (Model: LP-INFGRW), IngraGlow-White (Model: LP-INFGRWWHT); LED Red Therapy Light (Model: RL05-D, RL05-E, RL05-F, RL05-G, RL05-H, RL05-I), IngraGlow-White (Model: RL12-B), LED Red Therapy Light (Model: RL05-I); LED Red Therapy Light (Model: RL1000 MAX), LED Red Therapy Light (Model: RL1000 MAX+); LED Red Therapy Light (Model: RL1000 Plus) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer, Repackager or relabeler | 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 5, 2025 | K250467 | Red Light Hair Growth Cap (LP-RJVGRW-BLK) | OAP | Substantially Equivalent | Shenzhen Idea Light Limited | accessdata.fda.gov |
| January 12, 2024 | K233114 | LED silicone mask (Model: LP-RVTGLWP-WHT, LP-RVTGLW-WHT, TLM200) | OHS | Substantially Equivalent | Shenzhen Idea Light Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Massager, Therapeutic, Electric
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Laser, Comb, Hair
Updated June 5, 2025. 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.