Ryder Intl. Corp.: FDA clearances and approvals
Ryder Intl. Corp. has 10 FDA 510(k) clearances (first 1985, latest 1996), across 7 product codes in 3 review panels. Median 510(k) review time: 98 days.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LRX | Case, Contact Lens | 3 | 3 |
| HPX | Lens, Contact (Polymethylmethacrylate) | 2 | 2 |
| KOD | Catheter, Urological | 1 | 1 |
| KOE | Dilator, Urethral | 1 | 1 |
| LPN | Accessories, Soft Lens Products | 1 | 1 |
| MAV | Syringe, Balloon Inflation | 1 | 1 |
| OKS | Lacrimal Stents And Intubation Sets | 1 | 1 |
Review panels
Most recent Ryder Intl. Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K962611 | BARD EAGLE INFLATION DEVICE | KOE | 1996-10-21 | 110 |
| K962151 | RYDER LACRIMAL INTUBATIONSET | OKS | 1996-09-18 | 106 |
| K953522 | USCI IDEAL PTCA KIT | MAV | 1996-04-17 | 265 |
| K920064 | OPTI-LENS CONTACT LENS CASE | LRX | 1992-03-04 | 57 |
| K915082 | OPTI-LENS(TM) CONTACT LENS CASE | LRX | 1992-01-13 | 62 |
| K881981 | ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM | KOD | 1988-08-02 | 82 |
| K870278 | CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 | LPN | 1987-02-20 | 24 |
| K853727 | KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE) | LRX | 1986-02-07 | 154 |
| K853729 | KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE) | HPX | 1985-12-13 | 98 |
| K853728 | KESTREL CONTACT LENS STORAGE CASE(NORYL) | HPX | 1985-12-13 | 98 |
Recalls
openFDA lists no recalls under a recalling firm named Ryder Intl. Corp..
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Ryder Intl. Corp. have?
Ryder Intl. Corp. has 10 FDA 510(k) clearances (first 1985, latest 1996), across 7 product codes in 3 review panels.
How long does FDA take to clear Ryder Intl. Corp.'s 510(k)s?
The median time from FDA receipt to decision across Ryder Intl. Corp.'s cleared 510(k)s is 98 days.
What devices does Ryder Intl. Corp. make?
Its most frequent FDA product codes are LRX (Case, Contact Lens, 3); HPX (Lens, Contact (Polymethylmethacrylate), 2); KOD (Catheter, Urological, 1).
Has Ryder Intl. Corp. had device recalls?
openFDA lists no recalls under a recalling firm name matching Ryder Intl. Corp. Related entities may recall under other names.
Next steps
- See all 10 Ryder Intl. Corp. clearances with predicates and recalls
- Run predicate analysis for product code LRX, Ryder Intl. Corp.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.