Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Aap Implantate AG · Predicate Candidate Screening

37 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

109 daysmedian FDA review time
302 days90th percentile
37clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K254253LOQTEQ® VA Proximal Humerus Plate 3.5Aap Implantate AG2026-03-24850
K233008Cannulated Headless Bone ScrewsAap Implantate AG2024-06-052570
K230141LOQTEQ® VA Elbow Plates 2.7/3.5 SystemAap Implantate AG2023-03-17580
K211582LOQTEQ Proximal Humerus Plate 3.5 SystemAap Implantate AG2021-10-181500
K210043LOQTEQ Distal Lateral Femur Plate 4.5 SystemAap Implantate AG2021-03-03550
K182818LOQTEQ VA Calcaneus Plate 3.5Aap Implantate AG2019-08-013020
K182785LOQTEQ VA Foot Plates 2.5Aap Implantate AG2019-06-192610
K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG2016-11-231560
K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal MediAap Implantate AG2016-11-221510
K161703LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, WasherAap Implantate AG2016-11-041370
K153034aap LOQTEQ VA Radius Set 2.5Aap Implantate AG2016-01-21940
K150974aap Cortical Screw 1.5, self-tapping, aap Cortical Screw 1.5Aap Implantate AG2015-04-29160
K141949CORTICAL SCREW 3.5, T15, SELF-TAPPING, TITANIUM, CORTICAL SCAap Implantate AG2014-09-12560
K141823AAP LOQTEC CLAVICLE PLATES 2.7/3.5Aap Implantate AG2014-08-07310
K140607AAP LOQTEC(R) OLECRANON PLATEAap Implantate AG2014-05-08590
K133675AAP LOQTEQ DISTAL ANTEROLATERAL TIBIA PLATE 3.5Aap Implantate AG2014-01-23550
K132787LOQTEQ DISTAL DORSOLATERAL HUMERUS PLATEAap Implantate AG2013-12-241090
K131782LOQTEQ HIGH TIBIA OSTEOTOMY PLATE 4.5Aap Implantate AG2013-11-181540
K131459AAP K-WIRE, STEINMANN PIN, CERCLAGE WIREAap Implantate AG2013-10-171500
K132554AAP LOQTEQ PROXIMAL MEDIAL TIBIA PLATE 3.5Aap Implantate AG2013-10-03500
K130590AAP CANNULATED SCREW 2.0Aap Implantate AG2013-04-22460
K123875AAP RADIUS SET 2.5Aap Implantate AG2013-03-11840
K121495LOQTEQ PROXIMAL HUMERUS PLATE 3.5, SHORT LOQTEQ PROXIMAL HUMAap Implantate AG2012-12-072000
K121494LOQTEQ DISTAL LATERAL FEMUR PLATE 4.5 (LEFT AND RIGHT VERSIOAap Implantate AG2012-11-191820
K113601AAP LOQTEQ DISTAL MEDIAL TIBIA PLATE 3.5 SYSTEMAap Implantate AG2012-11-083390
K113602AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEMAap Implantate AG2012-10-313310
K113648LOQTEQ LARGE FRAGMENT SET LOQTEQ CORTICAL SCREW 4.5, SMALL HAap Implantate AG2012-09-062690
K113652LOQTEQ SMALL FRAGMENT SET LOQTEQ CORTICAL SCREW3.5, SMALL HEAap Implantate AG2012-08-302620
K111316AAP CANNULATED SCREWSAap Implantate AG2011-07-20710
K080101AAP CANNULATED SCREW AND DARCO HEADED SCREWAap Implantate AG2008-03-25710
K072411AAP BONE PLATES AND SCREW IMPLANTSAap Implantate AG2008-03-202060
K071852AAP APS SYSTEMAap Implantate AG2007-08-29550
K033260AEQUOSAap Implantate AG2004-12-074250
K030909AAP ACROPLATEAap Implantate AG2003-04-10170
K021233AAP CANNULATED SCREWSAap Implantate AG2002-12-092350
K021782BNFAap Implantate AG2002-08-26880
K990776AAP CANNULATED SCREW, 7.5MM, 4.5MM, 4.0MM, 3.5MM, 7.0MMAap Implantate AG1999-04-29510

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda