← Back to catalogue
K3Pro Konus Dental Implants
FDA UDIClass I (US FDA UDI)
by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG
Identity
- Trade Name
- K3Pro Konus Dental Implants FDA UDI
- Generic Name
- Dental implant/prosthesis surgical procedure kit FDA UDI
- Device Name
- K3Pro Basic Tray Sure FDA UDI
- Model / Reference
- SK01_K3Pro.ZB FDA UDI
- Description
- K3Pro Basic Tray Sure FDA UDI
Identifiers
- Catalog Number
- SK01_K3Pro.ZB FDA UDI
- Primary DI / UDI-DI
- EAGNSK01K3PROZB0 FDA UDI
- 510(k) Number
- K141159 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Dental implant/prosthesis surgical procedure kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental implant/prosthesis surgical procedure kit
K3Pro Konus Dental Implants by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Dental implant/prosthesis surgical procedure kit.
- STOP FOR CYLINDRICAL DRILL — SWEDEN & MARTINA INC · Class I
- RIGHT ANGLE BONE TAP — SWEDEN & MARTINA INC · Class I
- MILLABLE CRCO ABUTMENT — SWEDEN & MARTINA INC · Class I
- ANALOGUE FOR ABUTMENT — SWEDEN & MARTINA INC · Class I
- SELF THREAD/LOGIC PLUS/SPARK — Hi-Tec Implants · Class II
- SURGICAL INSTRUMENTATION — Hi-Tec Implants · Class II
- Guided Surgery — BICON, LLC · Class I
- ROUND TIP OSTEOTOME FOR GLOBAL — SWEDEN & MARTINA INC · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
Sources (1)
- FDA UDI a59fa523-7c44-450d-8bc2-774f29039fd6 36 fields · synced Jun 1, 2026