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Morelli
Dental Morelli Ltda · Model 30.45.003 · UDI-DI 07895742119973
ECO
Prescription
7
510(k) clearances
7
Adverse events
13
Recalls
82
Facilities
Description
Molar Distalizer Type Jones - Universal
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.