Aap Implantate AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Aap Implantate AG - FDA 510(k) Cleared Devices
Recent clearances: LOQTEQ® VA Proximal Humerus Plate 3.5, Cannulated Headless Bone Screws, LOQTEQ® VA Elbow Plates 2.7/3.5 System
37
Total
37
Cleared
0
Denied
Aap Implantate AG has 37 FDA 510(k) cleared orthopedic devices. Based in Berlin, DE.
Latest FDA clearance: Mar 2026. Active since 1999.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Aap Implantate AG
37 devices
Cleared
Mar 24, 2026
LOQTEQ® VA Proximal Humerus Plate 3.5
Orthopedic
85d
Cleared
Jun 05, 2024
Cannulated Headless Bone Screws
Orthopedic
257d
Cleared
Mar 17, 2023
LOQTEQ® VA Elbow Plates 2.7/3.5 System
Orthopedic
58d
Cleared
Oct 18, 2021
LOQTEQ Proximal Humerus Plate 3.5 System
Orthopedic
150d
Cleared
Mar 03, 2021
LOQTEQ Distal Lateral Femur Plate 4.5 System
Orthopedic
55d
Cleared
Aug 01, 2019
LOQTEQ VA Calcaneus Plate 3.5
Orthopedic
302d
Cleared
Jun 19, 2019
LOQTEQ VA Foot Plates 2.5
Orthopedic
261d
Cleared
Nov 23, 2016
aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5
Orthopedic
156d
Cleared
Nov 22, 2016
LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5
Orthopedic
151d
Cleared
Nov 04, 2016
LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, Washer
Orthopedic
137d
Cleared
Jan 21, 2016
aap LOQTEQ VA Radius Set 2.5
Orthopedic
94d
Cleared
Apr 29, 2015
aap Cortical Screw 1.5, self-tapping, aap Cortical Screw 1.5, self-tapping,...
Orthopedic
16d
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