# Linc Medipharm Limited (foreign exporter, Wuxi Jiangsu, CN): 13 new FDA device listings, incl. needle, hypodermic, single lumen

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Linc Medipharm Limited |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Wuxi Jiangsu, CN |
| New listings | 13 |
| Devices | Needle, Hypodermic, Single Lumen; Syringe, Antistick; Set, Administration, Intravascular; Syringe, Piston; Tubes, Vials, Systems, Serum Separators, Blood Collection; Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature |
| Product codes | FMI, MEG, FPA, FMF, JKA, FMK |
| Device classes | Class II |
| Medical specialties | General Hospital, Clinical Chemistry, General, Plastic Surgery |
| First new listing | 2026-08-26 |
| Latest new listing | 2026-09-02 |
| FDA registration number | 3039435934 |
| Registration expires | 2027-12-31 |

## Why this score
- 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.