Hosmer Dorrance Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K822632ELBOW PROSTHESISSeptember 14, 1982
K821704FRACTURE BRACINGJune 24, 1982
K801788HUMEROUS FRACTURE BRACE, ULNA FRACTUREAugust 7, 1980
K780892FRACTURE BRACINGJune 13, 1978
K780891POST-OPERATIVE HIP ORTHOSISJune 13, 1978
K780890CAPP TERMINAL DEVICEJune 13, 1978
K761312ORTHOTIC BRACINGJanuary 10, 1977
K761314FLEXION-BRAKING KNEE-SHIN ASSEMBLYJanuary 10, 1977
K7613134-BAR KNEE-SHIN SET-UPJanuary 10, 1977