Atlas FDA

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

Ostial Corporation — Predicate Candidate Screening

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

103 daysmedian FDA review time
195 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K152485FLASH Mini Ostial System - 3.0mm x 8mm x 135cm, FLASH Mini OOstial Corporation2016-02-161690
K150946FLASH Ostial System OTW-6.0mm x 12mm x 80cm, FLASH Ostial SyOstial Corporation2015-05-08300
K133861FLASH OSTIAL SYSTEM OTW-7.0MMX17MMX135CM, FLASH OSTIAL SYSTEOstial Corporation2014-07-021950
K131450FLASH MINI OSTIAL SYSTEM - 3.0MM X 135CM, FLASH MINI OSTIAL Ostial Corporation2013-08-06780
K122178FLASH-C PTCA BALLOON DILATATION CATHETER - 4MM X 14MM X 135COstial Corporation2012-10-11800
K122379FLASH PTA BALLOON DILATATION CATHETER - 4MM X 14MM X 135CM, Ostial Corporation2012-09-05300
K121175FLASH PTA BALLON DILATATION CATHETER-5MM X 19MM X 135CMOstial Corporation2012-06-29720
K113582ARCHSTENT BILIARY SYSTEMOstial Corporation2012-06-292070
K113775FLASH-C PTCA BALLOON DILATATION CATHETER- 4.0MM X 14MM X 135Ostial Corporation2012-06-291900
K120738FLASH PTA BALLOON DILATATION CATHETER-4.0X14MMX135CMOstial Corporation2012-03-29170
K111284FLASH-C PTCA BALLOON DILATION CATHETER - 5MM X 19MM X 135CM Ostial Corporation2011-08-171030
K102482FLASH PTA BALLOON DILATATION CATHETER 5MM X 19MM X 135CM; FLOstial Corporation2011-02-251790

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