Manufacturer and brand owner in Guangzhou, Guangdong, China. 2 device types, 2 products catalogued, 2 clearances.
Guangzhou Hehong Biotech Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Labware, Assisted Reproduction, Catheter, Assisted Reproduction. 2 of its products are catalogued under its own name. Its earliest product listing with the FDA dates from 2026.
Registration
FDA registration record for Guangzhou Hehong Biotech Co., Ltd. | Registered name | GUANGZHOU HEHONG BIOTECH CO., LTD. |
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3043639843 |
| FEI number | 3043639843 |
| DUNS | 419557208 |
| Establishment type | Manufacturer |
Location
Address of Guangzhou Hehong Biotech Co., Ltd. | City | Guangzhou |
| Province | Guangdong |
| Address | A zone, 2/F, Building A, Huazi Industrial Park, |
| Postal code | 511447 |
| Country | China |
From the Company
Published by the company on its own website, not by the FDA.
Information published by Guangzhou Hehong Biotech Co., Ltd. | Founded | 2017 |
| Employees | 100+ technical staff |
| Main products | Vitrification straw, IUI catheter (artificial insemination catheter), Oocyte aspiration needles, Embryo transfer catheter, Denuding pipette |
| Certifications | FDA, ISO 13485, Japanese Class II Medical Registration, Russian Class II Medical Registration, Egyptian Embassy Authentication, Iranian Embassy Authentication |
| Export markets | Europe, Middle East, Africa, Southeast Asia, South America (20+ countries) |
| OEM and ODM | Offered |
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.