Ryder Intl. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ryder Intl. Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Ryder Intl. Corp. has 10 FDA 510(k) cleared ophthalmic devices. Based in Arab, US.
Historical record: 10 cleared submissions from 1985 to 1996.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ryder Intl. Corp.
10 devices
Cleared
Oct 21, 1996
BARD EAGLE INFLATION DEVICE
Gastroenterology & Urology
110d
Cleared
Sep 18, 1996
RYDER LACRIMAL INTUBATIONSET
Ophthalmic
106d
Cleared
Apr 17, 1996
USCI IDEAL PTCA KIT
Cardiovascular
265d
Cleared
Mar 04, 1992
OPTI-LENS CONTACT LENS CASE
Ophthalmic
57d
Cleared
Jan 13, 1992
OPTI-LENS(TM) CONTACT LENS CASE
Ophthalmic
62d
Cleared
Aug 02, 1988
ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM
Gastroenterology & Urology
82d
Cleared
Feb 20, 1987
CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695
Ophthalmic
24d
Cleared
Feb 07, 1986
KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)
Ophthalmic
154d
Cleared
Dec 13, 1985
KESTREL CONTACT LENS STORAGE CASE(NORYL)
Ophthalmic
98d
Cleared
Dec 13, 1985
KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)
Ophthalmic
98d