Tontec Precision Plastics Technology (Shenzhen) Co., Ltd.
Registered establishment in Shenzhen, Guangdong, China. 1 device type.
Tontec Precision Plastics Technology (Shenzhen) Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms). Its earliest product listing with the FDA dates from 2017.
Registration
| Registered name | TONTEC PRECISION PLASTICS TECHNOLOGY (SHENZHEN) CO. LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3008283443 |
| FEI number | 3008283443 |
| Establishment type | Contract manufacturer, Manufacturer |
Location
| City | Shenzhen |
|---|---|
| Province | Guangdong |
| Address | 55 BUXIA ROAD, LIUYUE , HENGGANG |
| Postal code | 0000 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | Class 2 | Quick Connect SpO2 Clip, Pediatric, Quick Connect SpO2 Grip, Ped, 20/box, Quick Connect SpO2 Grip, Neo, 20/box, Quick Connect SpO2 Starter Kit, Quick Connect SpO2 Clip, Adult, Quick Connect SpO2 Grip, Infant, 20/box and 1 more | 2017 | 17 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 1982 |
|---|---|
| Employees | 1627 |
| Main products | Plastic injection molds, Plastic moldings |
| OEM and ODM | Offered |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
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