Ortho Technology, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K112707 | GENERATION C AESTHETIC SELF-LIGATING BRACKET SYSTEM | NJM | 2012-01-13 | View |
| 510(k) | K073045 | SAPPHIRE CERAMIC BRACKET | NJM | 2007-12-18 | View |
No matching devices.
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