Atlas FDA

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

Inion OY — Predicate Candidate Screening

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

90 daysmedian FDA review time
182 days90th percentile
14clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K251441Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS Inion OY2025-11-071820
K251472Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System; Inion CInion OY2025-07-11590
K203105Inion CompressOn ScrewInion OY2021-01-13900
K191764Inion BioRestoreInion OY2019-07-31300
K151360Inion Spinal Graft Containment SystemInion OY2015-10-061390
K133932INION FREEDOMPINInion OY2014-04-111090
K123672INION FREEDOMSCREW (ALTERNATIVE MARKETING NAME: INION OTPS FInion OY2013-02-27900
K122890INION CPS ORBITAL PLATESInion OY2013-01-291310
K090177INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTEInion OY2009-02-20280
K070998INION BIORESTOREInion OY2007-10-111850
K071464INION HEXALON BIODEGRADABLE ACL/PCL SCREWInion OY2007-08-03660
K070784INION BIORESTOREInion OY2007-07-241250
K062782INION ANCHRON PLUS BIODEGRADABLE ANCHOR SYSTEM, MODEL ANC-60Inion OY2006-11-09520
K051362INION ANCHRON BIODEGRADABLE ANCHOR SYSTEM, MODEL ANC-6000Inion OY2005-08-04710

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