# Shenzhen Lincond Technology Co.,Ltd. (manufacturer, Shenzhen Guangdong, CN): 4 new FDA device listings, incl. lamp, infrared, therapeutic heating

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Shenzhen Lincond Technology Co.,Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Shenzhen Guangdong, CN |
| New listings | 4 |
| Devices | Lamp, Infrared, Therapeutic Heating; Pad, Eye; Pack, Hot Or Cold, Reusable; Massager, Therapeutic, Electric |
| Product codes | ILY, HMP, IME, ISA |
| Device classes | Class I, Class II |
| Medical specialties | Physical Medicine, General, Plastic Surgery |
| Brand names | BRAND: Miji Mila; Multi-Function Red Light Therapy Belt , MODEL:MB501,MODEL:MB502; Red Light Therapy Foot Device; Red Light Therapy Shoes; Infrared Light Therapy Device; Near-Infrared Therapy Foot Pad; Remote Control Red Light Therapy Vibration Pad; Inflatable Support Led Heating Vibration Massage Belt; Infrared Light Therapy Blanket; MODEL:MT020,MT021,MT022,MT023,MT024,MT025,MT026,MT027,MT028,MT029,MT030,MT031,MT032,MT033,MT034,MT035,MT036,MT037,MT038; Vibration Massage Infrared Light Therapy Knee Pad; Heating Vibration Shoulder Wrap; Led Light Vibration Knee Pad; Red Light Therapy Knee Massage, MODEL:MK203 |
| First new listing | 2026-05-26 |
| Latest new listing | 2026-05-26 |
| FDA registration number | 3045978226 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.