Atlas FDA

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

Innovative Medical Technologies, Inc. · Predicate Candidate Screening

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

244 daysmedian FDA review time
589 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K220458UltraFlo-R Push Button Blood Collection SetInnovative Medical Technologies, Inc.2023-09-295890
K123987IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION Innovative Medical Technologies, Inc.2013-08-272440
K972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMInnovative Medical Technologies, Inc.1997-09-22420
K936087CARPAL BOXInnovative Medical Technologies, Inc.1994-10-203030
K904237RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEMInnovative Medical Technologies, Inc.1991-05-092340
K854194IMT ULTRASONIC STRIDE MONITORInnovative Medical Technologies, Inc.1986-05-021990

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