Atlas FDA

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

Inman Liebelt Corp. — Predicate Candidate Screening

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

81 daysmedian FDA review time
148 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K912211INTRAVASCULAR CATHETER SECURMENT DEVICEInman Liebelt Corp.1991-08-09810
K912146URETERAL CATHETER HOLDERInman Liebelt Corp.1991-07-26720
K905590UCEZ - STERILE LENS FOG REDUCTION DEVICEInman Liebelt Corp.1991-05-101480
K905583ILC FORCEPS PADSInman Liebelt Corp.1991-04-121210
K903611ILC LEG BAG HOLDERInman Liebelt Corp.1990-10-26780
K903610O.R. TIP CLEANERInman Liebelt Corp.1990-10-19710

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