# Micro-Energy Medical Technology Co., Ltd. (manufacturer, Shenzhen Guangdong, CN): 4 new FDA device listings, incl. accessories, catheter

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Micro-Energy Medical Technology Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Shenzhen Guangdong, CN |
| New listings | 4 |
| Devices | Accessories, Catheter; Guide, Needle, Surgical; Powered Laser Surgical Instrument; Massager, Therapeutic, Electric |
| Product codes | KGZ, GDF, GEX, ISA |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, Physical Medicine |
| Brand names | Hemo Luer Lock; Hemo Needle; Hemolase Fiber (Hemo-R-0.40-2.5/Hemo-R-0.60-2.5/Hemo-R-0.40-1.8/Hemo-R-0.60-1.8); MEIM Therapeutic Shockwave Massager (model: KineShock 10 / KineShock 20) |
| First new listing | 2026-06-30 |
| Latest new listing | 2026-08-11 |
| FDA registration number | 3042261306 |
| Registration expires | 2027-12-31 |

## 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: 2026-10-28T20:51:27.468Z.
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.