Medical Device Manufacturer · FI , 20101 Turku

Orion Corp. - FDA 510(k) Cleared Devices

21 submissions · 20 cleared · Since 1985

Total

Cleared

Denied

Orion Corp. has 20 FDA 510(k) cleared medical devices. Based in 20101 Turku, FI.

Historical record: 20 cleared submissions from 1985 to 1992. Primary specialty: Microbiology.

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

Orion Corp. is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Orion Corp.

21 devices

1-12 of 21

Cleared May 04, 1992

RUBALEX, MODIFICATION

K912391 · LQN

Microbiology · 346d

Cleared Apr 26, 1990

RESUBMITTED MODIFIED RUBALEX

DENTOCULT SM-STRIP MUTANS

MODIFIED CHLAMYSET ANTIGEN

K872744 · LJP

Microbiology · 74d

Cleared Sep 11, 1987

CHLAMYSET ANTIBODY EIA

K864457 · LJC

Microbiology · 303d

Cleared Sep 11, 1987

DENTOCULT-SM CULTURE-PADDLE

K872301 · JSI

Microbiology · 88d

Cleared Jun 10, 1987

ORICULT-N CULTURE-PADDLE

K872058 · JSI

Microbiology · 13d

Cleared Oct 29, 1986

IMMUNOCHEMICAL ASSAY APOLIPOPROTEIN B

K861882 · MSJ

Immunology · 167d

Orion Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Orion Corp.

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