FDA Registration
Active
🇨🇳 China
ANKLE BRACE, 100621-050, 100621-060, 100622-005, 100622-010, 100622-020, 100622-030, 100622-040, 100622-050, 100622-060.
Reg #: 3015532798
·
FEI: 3015532798
·
Expires 2025
Products
1
Proprietary Names
4
Establishment Types
2
Classifications
1
Registration Details
- Registration Name
- GUANGDONG PROVICE RONGYI OUTDOOR LTD
- Registration Number
- 3015532798
- FEI Number
- 3015532798
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- rd Floor,Building 5,Xinghe Industrial Limited Company,Dalongkeng,Huangdong,ZhenLong Town,Huiyang District,Huiz
- City
- Huizhou Guangdong
- Country
- CN
Owner / Operator
- Firm Name
- GUANGDONG PROVICE RONGYI OUTDOOR LTD
- Operator Number
- 10060796
- Address
- rd Floor,Building 5,Xinghe Industrial Limited Company, Dalongkeng,, Huangdong,ZhenLong Town,Huiyang District,Huizhou City
- City
- Huizhou
- State
- Guangdong
- Postal Code
- 516227
- Country
- CN
- Correspondent
- Yan Hong
US Agent
- Business Name
- REPF America LLC
- Contact Name
- Wilson Li
- Address
- 6510 S Academy Blvd
- City
- Co Spgs
- State
- CO
- ZIP
- 80916
- Country
- US
- [email protected]
- Phone
- 719 2013315
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Orthosis, Limb Brace | IQI | Class 1 | Physical Medicine | No | 2019-06-24 |
Proprietary Names
ANKLE BRACE, 100621-050, 100621-060, 100622-005, 100622-010, 100622-020, 100622-030, 100622-040, 100622-050, 100622-060.
ANKLE BRACE, 25001, 25002, 25003, 25005, 25007, 25008, 25009, 100621-005, 100621-010, 100621-020, 100621-030, 100621-040
Hybrid Night Splint (ADJUSTABLE NIGHT SPLINT 100624-020, 100624-040, 100626-000, 30014, 30016, 30000S.
Posterior Night Splint(PLANTAR FASCllTIS NIGHT SPLINT) 100627-020, 100627-030, 100627-040, 31003, 31005, 31007.
Establishment Types
Manufacture Medical Device
Export Device to the United States But Perform No Other Operation on Device