# L&K Biomed Co.,Ltd. (manufacturer, Yongin-SI Gyeonggi, KR): 3 new FDA device listings, incl. appliance, fixation, spinal intervertebral body

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | L&K Biomed Co.,Ltd. |
| Owner / operator | L&K Biomed Co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Yongin-SI Gyeonggi, KR |
| New listings | 3 |
| Devices | Appliance, Fixation, Spinal Intervertebral Body; Intervertebral Fusion Device With Bone Graft, Cervical |
| Product codes | KWQ, ODP |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| Brand names | 6911-1733S; 6609-4021; 6610-4021S; 6912-1739S; 6609-4015S; 6609-3513S; 6911-1729; 6914-1773 |
| First new listing | 2026-05-10 |
| Latest new listing | 2026-08-20 |
| FDA registration number | 3008285983 |
| 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: 2026-11-04T21:52:36.524Z.
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.