FDA Registration Active 🇰🇷 South Korea

LnK Lumbar Interbody Fusion Cage System Instrument Set

Reg #: 3008285983 · FEI: 3008285983 · Expires 2025
Products
1
Proprietary Names
21
Establishment Types
1
Classifications
1

Registration Details

Registration Name
L&K BIOMED CO.,LTD.
Registration Number
3008285983
FEI Number
3008285983
Status
Active
Expiry Year
2025
Initial Importer
No
Address
#101, 201, #202, 16-25, Dongbaekjungang-ro 16 beon-gil, Giheung-gu
City
Yongin-SI Gyeonggi
Country
KR

Owner / Operator

Firm Name
L&K BIOMED CO., LTD.
Operator Number
10033804
Address
#101, 201, 202, 16-25, Dongbaekjungang-ro,, 16 beon-gil, Giheung-gu
City
Youngin-si
State
Gyeonggi
Postal Code
17015
Country
KR
Correspondent
Kihyang Kim

US Agent

Business Name
ComplianceAcuity, Inc
Contact Name
Kevin Randall
Address
485 Clinton St, #888
City
Ridgeway
State
CO
ZIP
81432
Country
US
Phone
303 8280844

Products

Device Name Product Code
Passer, Wire, Orthopedic HXI

Proprietary Names

LnK Lumbar Interbody Fusion Cage System Instrument Set LnK Cervical Interbody Fusion Cage System Instrument Set CastleLoc-C Cervical Interbody Fusion Cage System Instrument Set PathLoc-L MIS Spinal System Instrument Set PathLoc-SI Joint Fusion System Instrument Set LnK Anterior Cervical Plate System Instrument Set LnK Spinal Fixation System Instrument Set CastleLoc-P Anterior Cervical Plate System Instrument Set LnK MIS Spinal System Instrument Set TranS1 MIS Spinal System Instrument Set LnK Posterior Cervical Fixation System Instrument Set TranS1 Anterior Cervical Plate System Instrument Set TranS1 Spinal Fixation System Instrument Set TranS1 Lumbar Interbody Fusion Cage System Instrument Set TranS1 Posterior Cervical Fixation System Instrument Set TranS1 Cervical Interbody Fusion Cage System Instrument Set CastleLoc-S Posterior Cervical Fixation System Instrument Set PathLoc-C Posterior Cervical Fixation System Instrument Set PathLoc-LC Lateral Cage Instrument Set FOCUS Wire LnK MIS Wire

Establishment Types

Manufacture Medical Device