Orthion Corp.
Orthion Corp. appears in FDA public data with 0 recalls, 11 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 14, 1983.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K832546 | MARK V HIGH VOLTAGE GALVANIC STIMULATORR | October 14, 1983 |
| K823155 | LAVATORY SEAT HEIGHTENER | November 5, 1982 |
| K823153 | BATH TUB SEAT & BATH BOARD | November 5, 1982 |
| K823154 | SHOWER STOOL W/HANDLES | November 5, 1982 |
| K823149 | OB TILT TABLE | November 5, 1982 |
| K823156 | COLLAPSABLE LAVATORY HEIGHTENER | November 5, 1982 |
| K823150 | SESAM TREATMENT TABLE | November 5, 1982 |
| K823152 | OB HELP ARM | November 5, 1982 |
| K823105 | RESI-WALKER | November 5, 1982 |
| K823151 | OB TRIPP TRANSPORT CHAIR | November 5, 1982 |
| K812701 | ORTHO-THERM INFRARED SENSOR | October 13, 1981 |