# Hlb Life Science Co., Ltd. (manufacturer, Anseong-si, Gyeonggi-do, KR): 3 new FDA device listings, incl. low dead space piston syringe

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Hlb Life Science Co., Ltd. |
| Owner / operator | HLB Life Science Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Anseong-si, Gyeonggi-do, KR |
| New listings | 3 |
| Devices | Low Dead Space Piston Syringe; Needle, Hypodermic, Single Lumen; Syringe, Piston |
| Product codes | QNQ, FMI, FMF |
| Device classes | Class II |
| Medical specialties | General Hospital |
| Brand names | Single use Syringe with or without Needle/Sofjec, CarePoint Precision; Single use Needle/Sofjec, CarePoint Precision |
| First new listing | 2026-06-11 |
| Latest new listing | 2026-06-11 |
| FDA registration number | 3030089798 |
| 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.