FDA Registration
Active
🇰🇷 South Korea
Point Drill
Reg #: 3003781339
·
FEI: 3003781339
·
Expires 2025
Products
1
Proprietary Names
49
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- Cybermed Inc.
- Registration Number
- 3003781339
- FEI Number
- 3003781339
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 6-26, Yuseong-daero 1205beon-gil, Yuseong-gu
- City
- Daejeon
- Country
- KR
Owner / Operator
- Firm Name
- Cybermed Inc.
- Operator Number
- 9048516
- Address
- 6-26, Yuseong-daero 1205beon-gil, Yuseong-gu
- City
- Daejeon
- State
- KR-NOTA
- Postal Code
- 34104
- Country
- KR
- Correspondent
- KIM CHEOL YOUNG
US Agent
- Business Name
- Withus Group Inc.
- Contact Name
- April Lee
- Address
- 106 Superior
- City
- Irvine
- State
- CA
- ZIP
- 92620
- Country
- US
- [email protected]
- Phone
- 909 2749971
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Drill, Dental, Intraoral | DZA | Class 1 | Dental | No | 2009-12-01 |
Proprietary Names
Point Drill
CS First Drill
Reborn Sinus KIT
Crestal Guide Drill
Guided Drill
CORE1 Guide KIT Simple
LS Carbide Bur
Cortical Drill
First Drill
T.A Drill
In2Guide Surgical Template
Reborn Master KIT Full
Guide Drill
CORE Master KIT (Short)
Initial Guide Drill
Anchor Drill
CORE1 Guide KIT
CORE Drill
Reverse Drill
Connecter-handpiece
CORE Master KIT (Mini & Short)
Remover Drill
CORE Master KIT Simple
CORE Master KIT Full
Reborn Universal Guide KIT
Osteoplasty Bur
CORE Universal Guide KIT
LS Diamond Bur
Mount(AOS)
Reborn Master KIT
Bone Flatter
ABT. Profiler
In2Guide Universal Kit
Connector-Rachet
Reborn Guide KIT
Initial Drill
CORE D Guide KIT
Lateral Guide Drill
Tap Drill
Lateral Drill
CORE Sinus Master KIT
CORE Master KIT
CORE Z Guide KIT
CORE Sinus KIT
CS Drill
CORE Master KIT (Mini)
CORE Universal Remover and Prosthetic KIT
Reborn Sinus Master KIT
Bone Profiler
Establishment Types
Manufacture Medical Device