FDA Registration
Active
🇺🇸 United States
CROWN DELTA CORP.
Reg #: 2431069
·
FEI: 2431069
·
Expires 2026
Products
6
Proprietary Names
6
Establishment Types
3
Classifications
6
Registration Details
- Registration Name
- CROWN DELTA CORP.
- Registration Number
- 2431069
- FEI Number
- 2431069
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 1520 FRONT ST.
- City
- Yorktown
- State
- NY
- ZIP
- 10598
- Country
- US
Regulatory Submissions
- 510(k) Number
- K930248
Owner / Operator
- Firm Name
- CROWN DELTA CORP.
- Operator Number
- 2431069
- Address
- 1520 FRONT ST., --
- City
- Yorktown Hgts
- State
- NY
- Postal Code
- 10598
- Country
- US
- Correspondent
- MARK P KONOPKA
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Material, Impression | ELW | Class 2 | Dental | No | 2008-07-07 |
| Orthosis, Moldable, Supportive, Skin Protective | MNE | Class 1 | Physical Medicine | No | 2007-11-28 |
| Elastomer, Silicone, For Scar Management | MDA | Class 1 | General, Plastic Surgery | No | 2008-07-03 |
| Cord, Retraction | MVL | Class U | Unknown | No | 2016-06-16 |
| Syringe, Restorative And Impression Material | EID | Class 1 | Dental | No | 2010-04-16 |
| Applicator, Resin | KXR | Class 1 | Dental | No | 2024-01-30 |
Proprietary Names
Podiatric Impression Material
Vinyl Silicone Material
Silicone Elastomer Putty
VPS Silicone Adhesive
Impression Material Syringe
ZerofloX
Establishment Types
Manufacture Medical Device
Manufacture Medical Device for Another Party (Contract Manufacturer)
Repack or Relabel Medical Device