Suzhou Tianlong Biotechnology Co., Ltd.
Registered establishment in Suzhou, Jiangsu, China. 5 device types.
Suzhou Tianlong Biotechnology Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Antigen, B. Pertussis, Dna-Reagents, Legionella and 3 other device types. Its earliest product listing with the FDA dates from 2022.
Registration
| Registered name | SUZHOU TIANLONG BIOTECHNOLOGY CO., LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3026312356 |
| FEI number | 3026312356 |
| Establishment type | Manufacturer |
Chinese Registration
| Chinese legal name | 苏州天隆生物科技有限公司 |
|---|---|
| Unified social credit code | 91320594699344092G |
| Source | NMPA UDI database |
Location
| City | Suzhou |
|---|---|
| Province | Jiangsu |
| Address | Building NE-33, Nanopolis, No.99 Jinjihu Avenue, Suzhou Industrial Park, China (Jiangsu) Pilot Free Trade Zone |
| Postal code | 215123 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Antigen, B. Pertussis | Class 1 | Bacillus Pertussis Nucleic Acid Detection Kit (Fluorescence PCR Method) | 2022 | 1 |
| Antisera, All Types, Shigella Spp. | Class 2 | Salmonella Enterica/Shigella Nucleic Acid Multiplex Detection Kit (Fluorescence PCR Method) | 2022 | 1 |
| Dna-Reagents, Legionella | Class 2 | Legionella Pneumophila Nucleic Acid Detection Kit (Fluorescence PCR Method) | 2022 | 1 |
| Kit, Identification, Neisseria Gonorrhoeae | Class 1 | CT/NG/UU/UP Nucleic Acid Multiplex Detection Kit, Neisseria Gonorrhoeae (NG) Nucleic Acid Detection Kit (Fluorescence PCR Method) | 2022 | 2 |
| Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test | Class 1 | Group B Streptococcus (GBS) Nucleic Acid Detection Kit (Fluorescence PCR Method) | 2022 | 2 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2009 |
|---|---|
| Main products | Nucleic acid extraction instruments, Gene amplification instruments, PCR instruments, Diagnostic reagents |
| Certifications | ISO 9001, ISO 13485 |
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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