Atlas FDA

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

Icotec AG — Predicate Candidate Screening

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

165 daysmedian FDA review time
270 days90th percentile
16clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252327CMORE® CT System; CMORE® CT System Navigated InstrumentsIcotec AG2025-11-121100
K242900VADER® Pedicle System and VADER®one Pedicle SystemIcotec AG2025-02-271570
K233215icotec Anterior Cervical Plate SystemIcotec AG2024-05-172340
K232792icotec Interbody Cage System (icotec Cervical Cage, icotec PIcotec AG2024-04-052070
K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AG2024-04-042060
K232628VADER® Pedicle SystemIcotec AG2024-02-261810
K230861VADER® Pedicle System Navigated InstrumentsIcotec AG2023-06-27900
K222789VADER® Pedicle System, G21 CementIcotec AG2023-01-091162
K201587icotec Anterior Cervical Plate SystemIcotec AG2020-10-151260
K200596G21 Cement, VADER® Pedicle SystemIcotec AG2020-10-132211
K200235KONG-TL VBR System, KONG-C VBR SystemIcotec AG2020-05-291200
K193423VADER®one Pedicle System MIS and LightMore® Pedicle System 6Icotec AG2020-05-221651
K192897icotec Cervical CageIcotec AG2020-03-201610
K190545VADER® one Pedicle System MIS and LightMore® Pedicle System Icotec AG2019-06-201081
K172480icotec Interbody Cage SystemIcotec AG2018-05-172740
K151977icotec Pedicle SystemIcotec AG2016-04-122700

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