Orion Corp.
Orion Corp. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1992.
Top product codes for Orion Corp.
Recent clearances by Orion Corp.
- K912391 — RUBALEX, MODIFICATION
- K901637 — RESUBMITTED MODIFIED RUBALEX
- K884650 — RESUBMITTED SCANORA
- K890199 — DENTOCULT SM-STRIP MUTANS
- K881505 — MAMEX DC MG11
- K881506 — MAMEX DC MAG MG12
- K874040 — MAMEX DC S SL10/MG14
- K872744 — MODIFIED CHLAMYSET ANTIGEN
- K864457 — CHLAMYSET ANTIBODY EIA
- K872301 — DENTOCULT-SM CULTURE-PADDLE
- K872058 — ORICULT-N CULTURE-PADDLE
- K861882 — IMMUNOCHEMICAL ASSAY APOLIPOPROTEIN B
- K861883 — IMMUNOCHEMICAL ASSAY OF APOLIPOPROTEIN A1
- K863730 — MYOLEX
- K862671 — MICROALBUMINURIA ASSAY
- K860679 — IMMUNOCHEMICAL ASSAY OF C-REACTIVE PROTEIN
- K861881 — RUBALEX (REVISED VERSION)
- K853401 — CHLAMYSET ANTIGEN
- K852788 — RUBALEX
- K860529 — ROTALEX
- K851164 — DENTOCULT CULTURE-PADDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.