LEONE SPA
LEONE SPA · Model A1730-09 · UDI-DI 08033707001454
ECO
Prescription
7
510(k) clearances
7
Adverse events
13
Recalls
82
Facilities
Description
MEMORIA SPRINGS FIRST CLASS .
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
| 2018-05-01 | TP Orthodontics, Inc. | The firm has received 106 complaints of the device breaking in the patient's mouth. Device breakage may cause injury to the patient. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.