Medical Device Manufacturer · US , Mchenry , IL

Hosmer Dorrance Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1977

Total

Cleared

Denied

Hosmer Dorrance Corp. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1977 to 1982. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Hosmer Dorrance Corp. Filter by specialty or product code using the sidebar.

Hosmer Dorrance Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hosmer Dorrance Corp.

9 devices

1-9 of 9

Cleared Sep 14, 1982

ELBOW PROSTHESIS

K822632 · IRE

Physical Medicine · 14d

Cleared Jun 24, 1982

FRACTURE BRACING

K821704 · IQI

Physical Medicine · 22d

Cleared Aug 07, 1980

HUMEROUS FRACTURE BRACE, ULNA FRACTURE

K801788 · IQI

Physical Medicine · 9d

Cleared Jun 13, 1978

CAPP TERMINAL DEVICE

K780890 · IQX

Physical Medicine · 13d

Cleared Jun 13, 1978

POST-OPERATIVE HIP ORTHOSIS

K780891 · ITS

Physical Medicine · 13d

Cleared Jun 13, 1978

FRACTURE BRACING

K780892 · ITQ

Physical Medicine · 13d

Cleared Jan 10, 1977

ORTHOTIC BRACING

K761312 · IQI

Physical Medicine · 18d

Cleared Jan 10, 1977

4-BAR KNEE-SHIN SET-UP

K761313 · ION

Physical Medicine · 28d

Cleared Jan 10, 1977

FLEXION-BRAKING KNEE-SHIN ASSEMBLY

K761314 · ION

Physical Medicine · 18d

Hosmer Dorrance Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Hosmer Dorrance Corp.

Filters