FDA Registration
Active
🇧🇪 Belgium
RUNLITE S.A.
Reg #: 8020160
·
FEI: 6347
·
Expires 2026
Products
6
Proprietary Names
2
Establishment Types
1
Classifications
6
Registration Details
- Registration Name
- RUNLITE S.A.
- Registration Number
- 8020160
- FEI Number
- 6347
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 9 AVENUE DE LA COOPERATION, MICHEROUX
- City
- SOUMAGNE Liege
- Country
- BE
Owner / Operator
- Firm Name
- RUNLITE SA
- Operator Number
- 8020160
- Address
- N174W21475 Alcan Drive
- City
- Jackson
- State
- WI
- Postal Code
- 53037
- Country
- US
- Correspondent
- Lori Kalsow
US Agent
- Business Name
- Kinetec USA, Inc.
- Contact Name
- Lori Kalsow
- Address
- N174W21475 Alcan Drive
- City
- Jackson
- State
- WI
- ZIP
- 53037
- Country
- US
- [email protected]
- Phone
- 262 6771248 ext. 109
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Joint, Hip, External Brace | ITS | Class 1 | Physical Medicine | No | 1989-07-20 |
| Component, Cast | LGF | Class 1 | Orthopedic | No | 1989-07-20 |
| Bandage, Cast | ITG | Class 1 | Physical Medicine | No | 1987-04-03 |
| Orthosis, Limb Brace | IQI | Class 1 | Physical Medicine | No | 1989-07-20 |
| Joint, Ankle, External Brace | ITW | Class 1 | Physical Medicine | No | 1989-07-20 |
| Splint, Extremity, Noninflatable, External, Sterile | FYH | Class 1 | General, Plastic Surgery | No | 1987-04-03 |
Proprietary Names
3D-Lite
X-Lite
Establishment Types
Manufacture Medical Device