Medical Device Manufacturer · US , Mchenry , IL

Loredan Biomedical, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1983

Total

Cleared

Denied

Loredan Biomedical, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1983 to 1993. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Loredan Biomedical, Inc. Filter by specialty or product code using the sidebar.

Loredan Biomedical, Inc. 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 - Loredan Biomedical, Inc.

9 devices

1-9 of 9

Cleared May 12, 1993

LIDO V-TAK

K924512 · LXJ

Physical Medicine · 250d

Cleared Mar 31, 1993

LIDO(R) LINEA

K924513 · BXB

Physical Medicine · 208d

Cleared Aug 14, 1990

LIDO LINEA

K903429 · IKK

Physical Medicine · 14d

Cleared Nov 18, 1988

LIDO TM ACTIVE BACK

K884487 · IKK

Physical Medicine · 24d

Cleared Feb 26, 1988

LIDO(TM) LIFT

K880017 · IKK

Physical Medicine · 52d

Cleared Feb 26, 1988

LIDO(TM) WORKSET

K880018 · IKK

Physical Medicine · 52d

Cleared Jun 05, 1987

LIDO ACTIVE

K871793 · IKK

Physical Medicine · 29d

Cleared Jun 02, 1986

LIDO BACK

K861986 · IKK

Physical Medicine · 11d

Cleared Sep 26, 1983

LANE ONE

K832770 · IKK

Physical Medicine · 41d

Loredan Biomedical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Loredan Biomedical, Inc.

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