Ortho Source
FDA 510(k) & PMA Approved Devices — 9 products
Advertisement
Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K913853 | FISSURE SEALER | EBC | 1992-08-27 | View |
| 510(k) | K913854 | ORTHO LIGHT CURE | DYH | 1992-01-14 | View |
| 510(k) | K913519 | SUMO GLASS IONOMER CEMENT | EMA | 1991-11-19 | View |
| 510(k) | K884949 | VISIBLE LIGHT CURE CALCIUM HYDROXIDE LINER | EJK | 1989-02-23 | View |
| 510(k) | K884575 | MAXIBOND | DYH | 1989-01-03 | View |
| 510(k) | K861118 | ORTHOJOIN, ORTHODONTIC ADHESIVE | DYH | 1986-05-02 | View |
| 510(k) | K861258 | PERMABAND (ORTHODONTIC ADHESIVE) | DYH | 1986-04-17 | View |
| 510(k) | K861245 | ORTHOSOURCE ETCH SYSTEMS | EBC | 1986-04-11 | View |
| 510(k) | K860959 | DEPENDABOND | DYH | 1986-03-25 | View |
No matching devices.
Advertisement