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Orthion Corp.

FDA Regulatory Profile

Orthion Corp. has 0 FDA recalls, 0 inspections, 11 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Oct 14, 1983

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances11Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K832546MARK V HIGH VOLTAGE GALVANIC STIMULATORROct 14, 1983
K823150SESAM TREATMENT TABLENov 5, 1982
K823155LAVATORY SEAT HEIGHTENERNov 5, 1982
K823153BATH TUB SEAT & BATH BOARDNov 5, 1982
K823149OB TILT TABLENov 5, 1982
K823152OB HELP ARMNov 5, 1982
K823156COLLAPSABLE LAVATORY HEIGHTENERNov 5, 1982
K823154SHOWER STOOL W/HANDLESNov 5, 1982
K823105RESI-WALKERNov 5, 1982
K823151OB TRIPP TRANSPORT CHAIRNov 5, 1982
K812701ORTHO-THERM INFRARED SENSOROct 13, 1981

FDA data resources