U.S. Toy Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U.S. Toy Co., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
U.S. Toy Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 5 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by U.S. Toy Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - U.S. Toy Co., Inc.
5 devices
Cleared
Nov 02, 1993
ANIMAL NONPRESCRIPTION SUNGLASSES
Ophthalmic
81d
Cleared
Nov 02, 1993
AVIATOR NONPRESCRIPTION SUNGLASSES
Ophthalmic
81d
Cleared
Nov 02, 1993
BUTTERFLY NONPRESCRIPTION SUNGLASSES
Ophthalmic
81d
Cleared
Nov 02, 1993
CHILD NONPRESCRIPTION SUNGLASSES
Ophthalmic
81d
Cleared
Nov 02, 1993
DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES
Ophthalmic
81d