Atlas FDA

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

Ryder Intl. Corp. — Predicate Candidate Screening

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

98 daysmedian FDA review time
265 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K962611BARD EAGLE INFLATION DEVICERyder Intl. Corp.1996-10-211100
K962151RYDER LACRIMAL INTUBATIONSETRyder Intl. Corp.1996-09-181060
K953522USCI IDEAL PTCA KITRyder Intl. Corp.1996-04-172650
K920064OPTI-LENS CONTACT LENS CASERyder Intl. Corp.1992-03-04570
K915082OPTI-LENS(TM) CONTACT LENS CASERyder Intl. Corp.1992-01-13620
K881981ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEMRyder Intl. Corp.1988-08-02820
K870278CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695Ryder Intl. Corp.1987-02-20240
K853727KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)Ryder Intl. Corp.1986-02-071540
K853729KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)Ryder Intl. Corp.1985-12-13980
K853728KESTREL CONTACT LENS STORAGE CASE(NORYL)Ryder Intl. Corp.1985-12-13980

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