Atlas FDA

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

Corventis, Inc. — Predicate Candidate Screening

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

65 daysmedian FDA review time
112 days90th percentile
7clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K133701NUVANT MCT SYSTEMCorventis, Inc.2014-02-06650
K113372NUVANT, MOBILC CARDIAC TELEMETRYCorventis, Inc.2012-03-071120
K113187AVIVO MOBILE PATIENT MANAGEMENTCorventis, Inc.2012-01-04650
K111917NUVANT, MOBILE CARDIAC TELEMETRYCorventis, Inc.2011-08-24490
K091971AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIACorventis, Inc.2009-08-27570
K090696NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIACorventis, Inc.2009-06-19950
K083287AVIVO MOBILE PATIENT MANAGEMENT SYSTEMCorventis, Inc.2009-02-03880

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