ClearanceBrief
Company ยท US

Hosmer Dorrance Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1982. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IQIOrthosis, Limb Brace3
IONExerciser, Non-Measuring2
IQXHook, External Limb Component, Mechanical1
IREJoint, Elbow, External Limb Component, Powered1
ITQJoint, Knee, External Brace1
ITSJoint, Hip, External Brace1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 14, 1982K822632ELBOW PROSTHESIS
Hosmer Dorrance Corp.
IRE
Jun 24, 1982K821704FRACTURE BRACING
Hosmer Dorrance Corp.
IQI
Aug 7, 1980K801788HUMEROUS FRACTURE BRACE, ULNA FRACTURE
Hosmer Dorrance Corp.
IQI
Jun 13, 1978K780892FRACTURE BRACING
Hosmer Dorrance Corp.
ITQ
Jun 13, 1978K780891POST-OPERATIVE HIP ORTHOSIS
Hosmer Dorrance Corp.
ITS
Jun 13, 1978K780890CAPP TERMINAL DEVICE
Hosmer Dorrance Corp.
IQX
Jan 10, 1977K761314FLEXION-BRAKING KNEE-SHIN ASSEMBLY
Hosmer Dorrance Corp.
ION
Jan 10, 1977K7613134-BAR KNEE-SHIN SET-UP
Hosmer Dorrance Corp.
ION
Jan 10, 1977K761312ORTHOTIC BRACING
Hosmer Dorrance Corp.
IQI

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes