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Begg Rotating Springs
TP ORTHODONTICS INC · Model 240-101 · UDI-DI 00192029049600
7
510(k) clearances
7
Adverse events
13
Recalls
82
Facilities
Description
CCW Medium
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.