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-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K254253 | LOQTEQ® VA Proximal Humerus Plate 3.5 | Aap Implantate AG | 2026-03-24 | 85 | 0 |
| K233008 | Cannulated Headless Bone Screws | Aap Implantate AG | 2024-06-05 | 257 | 0 |
| K230141 | LOQTEQ® VA Elbow Plates 2.7/3.5 System | Aap Implantate AG | 2023-03-17 | 58 | 0 |
| K211582 | LOQTEQ Proximal Humerus Plate 3.5 System | Aap Implantate AG | 2021-10-18 | 150 | 0 |
| K210043 | LOQTEQ Distal Lateral Femur Plate 4.5 System | Aap Implantate AG | 2021-03-03 | 55 | 0 |
| K182818 | LOQTEQ VA Calcaneus Plate 3.5 | Aap Implantate AG | 2019-08-01 | 302 | 0 |
| K182785 | LOQTEQ VA Foot Plates 2.5 | Aap Implantate AG | 2019-06-19 | 261 | 0 |
| K161696 | aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5 | Aap Implantate AG | 2016-11-23 | 156 | 0 |
| K161747 | LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medi | Aap Implantate AG | 2016-11-22 | 151 | 0 |
| K161703 | LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, Washer | Aap Implantate AG | 2016-11-04 | 137 | 0 |
| K153034 | aap LOQTEQ VA Radius Set 2.5 | Aap Implantate AG | 2016-01-21 | 94 | 0 |
| K150974 | aap Cortical Screw 1.5, self-tapping, aap Cortical Screw 1.5 | Aap Implantate AG | 2015-04-29 | 16 | 0 |
| K141949 | CORTICAL SCREW 3.5, T15, SELF-TAPPING, TITANIUM, CORTICAL SC | Aap Implantate AG | 2014-09-12 | 56 | 0 |
| K141823 | AAP LOQTEC CLAVICLE PLATES 2.7/3.5 | Aap Implantate AG | 2014-08-07 | 31 | 0 |
| K140607 | AAP LOQTEC(R) OLECRANON PLATE | Aap Implantate AG | 2014-05-08 | 59 | 0 |
| K133675 | AAP LOQTEQ DISTAL ANTEROLATERAL TIBIA PLATE 3.5 | Aap Implantate AG | 2014-01-23 | 55 | 0 |
| K132787 | LOQTEQ DISTAL DORSOLATERAL HUMERUS PLATE | Aap Implantate AG | 2013-12-24 | 109 | 0 |
| K131782 | LOQTEQ HIGH TIBIA OSTEOTOMY PLATE 4.5 | Aap Implantate AG | 2013-11-18 | 154 | 0 |
| K131459 | AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE | Aap Implantate AG | 2013-10-17 | 150 | 0 |
| K132554 | AAP LOQTEQ PROXIMAL MEDIAL TIBIA PLATE 3.5 | Aap Implantate AG | 2013-10-03 | 50 | 0 |
| K130590 | AAP CANNULATED SCREW 2.0 | Aap Implantate AG | 2013-04-22 | 46 | 0 |
| K123875 | AAP RADIUS SET 2.5 | Aap Implantate AG | 2013-03-11 | 84 | 0 |
| K121495 | LOQTEQ PROXIMAL HUMERUS PLATE 3.5, SHORT LOQTEQ PROXIMAL HUM | Aap Implantate AG | 2012-12-07 | 200 | 0 |
| K121494 | LOQTEQ DISTAL LATERAL FEMUR PLATE 4.5 (LEFT AND RIGHT VERSIO | Aap Implantate AG | 2012-11-19 | 182 | 0 |
| K113601 | AAP LOQTEQ DISTAL MEDIAL TIBIA PLATE 3.5 SYSTEM | Aap Implantate AG | 2012-11-08 | 339 | 0 |
| K113602 | AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM | Aap Implantate AG | 2012-10-31 | 331 | 0 |
| K113648 | LOQTEQ LARGE FRAGMENT SET LOQTEQ CORTICAL SCREW 4.5, SMALL H | Aap Implantate AG | 2012-09-06 | 269 | 0 |
| K113652 | LOQTEQ SMALL FRAGMENT SET LOQTEQ CORTICAL SCREW3.5, SMALL HE | Aap Implantate AG | 2012-08-30 | 262 | 0 |
| K111316 | AAP CANNULATED SCREWS | Aap Implantate AG | 2011-07-20 | 71 | 0 |
| K080101 | AAP CANNULATED SCREW AND DARCO HEADED SCREW | Aap Implantate AG | 2008-03-25 | 71 | 0 |
| K072411 | AAP BONE PLATES AND SCREW IMPLANTS | Aap Implantate AG | 2008-03-20 | 206 | 0 |
| K071852 | AAP APS SYSTEM | Aap Implantate AG | 2007-08-29 | 55 | 0 |
| K033260 | AEQUOS | Aap Implantate AG | 2004-12-07 | 425 | 0 |
| K030909 | AAP ACROPLATE | Aap Implantate AG | 2003-04-10 | 17 | 0 |
| K021233 | AAP CANNULATED SCREWS | Aap Implantate AG | 2002-12-09 | 235 | 0 |
| K021782 | BNF | Aap Implantate AG | 2002-08-26 | 88 | 0 |
| K990776 | AAP CANNULATED SCREW, 7.5MM, 4.5MM, 4.0MM, 3.5MM, 7.0MM | Aap Implantate AG | 1999-04-29 | 51 | 0 |
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