FDA Device Intelligence
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Spring, Orthodontic

FDA product code ECO · Class 1 · Dental

916
Registered devices
7
Adverse events
13
Recalls
7
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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.
2018-05-01TP 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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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.