FDA Registration
Active
🇺🇸 United States
CORONET® DMEK EndoGlide
Reg #: 3008719017
·
FEI: 3008719017
·
Expires 2025
Products
1
Proprietary Names
1
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- SUMMIT MEDICAL LLC
- Registration Number
- 3008719017
- FEI Number
- 3008719017
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- Yes
- Address
- 815 Vikings Pkwy Ste 100
- City
- Saint Paul
- State
- MN
- ZIP
- 55121
- Country
- US
Owner / Operator
- Firm Name
- Summit Medical, LLC
- Operator Number
- 10033920
- Address
- 815 Vikings Parkway, Suite 100
- City
- Saint Paul
- State
- MN
- Postal Code
- 55121
- Country
- US
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Spatula, Ophthalmic | HND | Class 1 | Ophthalmic | No | 2024-09-23 |
Proprietary Names
CORONET® DMEK EndoGlide
Establishment Types
Complaint File Establishment per 21 CFR 820.198