FDA Registration
Active
🇺🇸 United States
PURETEK CORPORATION
Reg #: 3012818008
·
FEI: 3012818008
·
Expires 2026
Products
4
Proprietary Names
3
Establishment Types
1
Classifications
4
Registration Details
- Registration Name
- PURETEK CORPORATION
- Registration Number
- 3012818008
- FEI Number
- 3012818008
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- Yes
- Address
- 7900 NELSON RD STE A
- City
- Panorama City
- State
- CA
- ZIP
- 91402
- Country
- US
Owner / Operator
- Firm Name
- PureTek Corporation
- Operator Number
- 10052870
- Address
- 7900 Nelson Road, Suite A
- City
- Panorama City
- State
- CA
- Postal Code
- 91402
- Country
- US
- Correspondent
- Elaine Matic
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Silicone Hydrogel For Scar Management | PFP | Class 1 | General, Plastic Surgery | No | 2020-12-22 |
| Gauze / Sponge,Nonresorbable For External Use | NAB | Class 1 | General, Plastic Surgery | No | 2020-04-09 |
| Tape And Bandage, Adhesive | KGX | Class 1 | General Hospital | No | 2020-05-18 |
| Elastomer, Silicone, For Scar Management | MDA | Class 1 | General, Plastic Surgery | No | 2020-05-19 |
Proprietary Names
Silagel
DermacinRx
Silicon Sheet
Establishment Types
Repack or Relabel Medical Device