Shenzhen Tonycore Technology Co., Ltd.
Registered establishment in Shenzhen, Guangdong, China. 4 device types.
Shenzhen Tonycore Technology Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Hearing Aid, Air-Conduction, Prescription, Hearing Aid, Air-Conduction, Over The Counter and 2 other device types. Its earliest product listing with the FDA dates from 2022.
Registration
| Registered name | SHENZHEN TONYCORE TECHNOLOGY CO.,LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3025427079 |
| FEI number | 3025427079 |
| Establishment type | Contract manufacturer, Complaint-file establishment, Manufacturer, Exporter |
Location
| City | Shenzhen |
|---|---|
| Province | Guangdong |
| Address | Room 808, Xinlong Building, Minzhi Street, Longhua District |
| Postal code | 518131 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | Class 2 | Clearwaves Hearing Aids Essential G010, Clearwaves App, G018 G019 G020 G021 G022 G023 G024 G025 G026 G027 G028 G029 G030, Hearing Aid, Amplifiers With Models G001 G002 G003 G004 G005 G006 G007 G008 G009 G010 G011 G012 G013 G014 G015 G016 G017 | 2023 | 52 |
| Hearing Aid, Air-Conduction With Wireless Technology, Prescription | Class 2 | T016 T017 T018 T019 T020 T021 T022 T023 T024 T025 T026 T027 T028 T029 T030, Wireless Bluetooth Hearing Aid/Amplifier T001 T002 T003 T004 T005 T006 T007 T008 T009 T010 T011 T012 T013 T014 T015 | 2022 | 29 |
| Hearing Aid, Air-Conduction, Over The Counter | Class 1 | D017 D018 D019 D020 D021 D022 D023 D024 D025 D026 D027 D028 D029 D030, Hearing Aid, Amplifiers With Models D001 D002 D003 D004 D005 D006 D007 D008 D009 D010 D011 D012 D013 D014 D015 D016 | 2023 | 57 |
| Hearing Aid, Air-Conduction, Prescription | Class 1 | Hearing Aid, Amplifiers With Models H001 H002 H003 H004 H005 H006 H007 H008 H009 H010 H011 H012 H013 H014 H015 H016, H017 H018 H019 H020 H021 H022 H023 H024 H025 H026 H027 H028 H029 H030 | 2023 | 45 |
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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.
The manufacturer named here can complete this record.