Medical Device Manufacturer · US , Houston , TX

Henley Intl. - FDA 510(k) Cleared Devices

44 submissions · 41 cleared · Since 1986

Total

Cleared

Denied

Henley Intl. has 41 FDA 510(k) cleared medical devices. Based in Houston, US.

Historical record: 41 cleared submissions from 1986 to 1995. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Henley Intl. Filter by specialty or product code using the sidebar.

Henley Intl. 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 - Henley Intl.

44 devices

1-12 of 44

Cleared Nov 15, 1995

NEUROLOGICAL DIAGNOSTIC DEVICES

Physical Medicine · 507d

Cleared May 05, 1994

UPPER BODY EXERCISER

K926279 · ISD

Physical Medicine · 507d

Cleared Mar 22, 1994

EXERCISE BICYCLE

K926287 · ISD

Physical Medicine · 463d

Cleared Mar 18, 1994

HYDRA FITNESS MODEL 311 TOTAL POWER

K926314 · ISD

Physical Medicine · 458d

Cleared Feb 04, 1994

COMPUTERIZED TESTING AND EXERCISE SYSTEMS

K926313 · BXB

Physical Medicine · 416d

Cleared Jul 21, 1993

MONOTRODE CUTANEOUS ELECTRODE

Physical Medicine · 424d

Cleared Mar 24, 1993

TRUE-TRAC, STRATUS

K926316 · JFB

Physical Medicine · 99d

Cleared Mar 09, 1993

SONOPULS 590

K920983 · IMI

Physical Medicine · 372d

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Henley Intl. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Henley Intl.

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