Waldemar Link GmbH & Co. KG - FDA 510(k) Cleared Devices
42
Total
42
Cleared
0
Denied
Waldemar Link GmbH & Co. KG has 42 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Latest FDA clearance: Nov 2025. Active since 1978. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Waldemar Link GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Waldemar Link GmbH & Co. KG
18 devices
Cleared
Nov 05, 2025
Allure Hip Stem and Intramedullary Plugs
Orthopedic
268d
Cleared
May 16, 2025
MobileLink Acetabular Cup System - inhouse coatings
Orthopedic
147d
Cleared
Nov 08, 2024
MobileLink Acetabular Cup System - Line Extension (Multiple)
Orthopedic
155d
Cleared
Nov 16, 2023
LINK Embrace Shoulder System - Reverse Configuration
Orthopedic
182d
Cleared
Apr 14, 2023
LINK MobileLink Acetabular Cup System
Orthopedic
275d
Cleared
Mar 21, 2023
LinkSymphoKnee – Fixed Bearing Ultracongruent (FB UC) Articulating Surface
Orthopedic
28d
Cleared
Sep 13, 2022
SP-CL Hip Stem and LCU Hip System
Orthopedic
285d
Cleared
Jul 20, 2022
Vario-Cup System
Orthopedic
29d
Cleared
Jun 03, 2022
BiMobile Instruments (for BiMobile Dual Mobility System)
Orthopedic
378d
Cleared
May 03, 2022
LINK Endo-Model EVO Knee System
Orthopedic
60d
Cleared
Apr 11, 2022
MP Reconstruction System
Orthopedic
140d
Cleared
Nov 18, 2021
LINK® Embrace Shoulder System - Reverse Configuration
Orthopedic
59d