FDA Registration
Active
🇨🇳 China
ZHEJIANG HINDAR OPTICAL CO.,LTD
Reg #: 9615473
·
FEI: 3000265857
·
Expires 2026
Products
8
Proprietary Names
5
Establishment Types
10
Classifications
8
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Registration Details
- Registration Name
- ZHEJIANG HINDAR OPTICAL CO.,LTD
- Registration Number
- 9615473
- FEI Number
- 3000265857
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 518# JIGUANG RD LOUQIAO STREET, OUHAI DISTRICT
- City
- wenzhou Zhejiang
- Country
- CN
Owner / Operator
- Firm Name
- ZHEJIANG HINDAR OPTICAL CO.,LTD
- Operator Number
- 10024906
- Address
- 518# JIGUANG RD LOUQIAO STREET, OUHAI DISTRICT
- City
- WENZHOU
- State
- Zhejiang
- Postal Code
- 325000
- Country
- CN
- Correspondent
- Beatrice Pan
US Agent
- Business Name
- J & F Technology Service
- Contact Name
- Fanny Zhao
- Address
- 19838 Moon Shadow Circle
- City
- Walnut
- State
- CA
- ZIP
- 91789
- Country
- US
- [email protected]
- Phone
- 909 5100201
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Mask, Scavenging | KHA | Class 1 | Anesthesiology | No | 2020-03-30 |
| Lens, Spectacle, Non-Custom (Prescription) | HQG | Class 1 | Ophthalmic | No | 2018-06-13 |
| Accessory, Surgical Apparel | LYU | Class 1 | General, Plastic Surgery | No | 2020-03-30 |
| Spectacle, Magnifying | HOI | Class 1 | Ophthalmic | No | 2009-07-24 |
| Lens, Spectacle (Prescription), For Reading Discomfort | NJH | Class 1 | Ophthalmic | No | 2008-03-01 |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | Class 1 | Ophthalmic | No | 2008-03-01 |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | Class 1 | Ophthalmic | No | 2020-03-03 |
| Frame, Spectacle | HQZ | Class 1 | Ophthalmic | No | 2008-03-01 |
Proprietary Names
ZheJiang Hindar Optical Co., Ltd
ZHEJIANG HINDAR OPTICAL CO.,LTD
Wenzhou Chuangyu Eyewear Co.,Ltd
Wenzhou Hongge optical co.,ltd.
Wenzhou Sanma Glasses Co., Ltd.
Establishment Types
Remanufacture Medical Device
Foreign Private Label Distributor
Complaint File Establishment per 21 CFR 820.198
Sterilize Medical Device for Another Party (Contract Sterilizer)
Repack or Relabel Medical Device
Develop Specifications But Do Not Manufacture At This Facility
Manufacture Medical Device
Manufacture Medical Device for Another Party (Contract Manufacturer)
Reprocess Single-Use Device
Export Device to the United States But Perform No Other Operation on Device