Identity
- Trade Name
- Basic-S Kit FDA UDI
- Generic Name
- Dental ultrasonic surgical system handpiece tip FDA UDI
- Model / Reference
- Basic-S Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560264563056 FDA UDI
- 510(k) Number
- K073678 FDA UDI
- FDA Product Code
- DZI FDA UDIELC FDA UDI
- GMDN Term
- Dental ultrasonic surgical system handpiece tip FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.4120 FDA UDI872.4850 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
No
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 ultrasonic surgical system handpiece tip
Basic-S Kit by Nakanishi Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental ultrasonic surgical system handpiece tip.
- MECTRON — MECTRON SPA · Class II
- ACTEON — Satelec · Class II
- CI Tip — B&L Biotech Co., Ltd. · Class I
- MECTRON — MECTRON SPA · Class II
- ACTEON — Satelec · Class II
- Vista CT4 (Thin Condensation) Apical Surgery P5 Tip — Vista Dental · Class I
- PIEZON MASTER SURGERY — E.M.S. Electro Medical Systems S.A. · Class II
- PIEZON MASTER SURGERY — E.M.S. Electro Medical Systems S.A. · Class II
Cleared under the same submission
K073678 also covers:
- Bone Cut Kit — NAKANISHI INC.
- Endo-S Kit — NAKANISHI INC.
- Implant Preparation Kit — NAKANISHI INC.
- Sinus Lift Kit — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
- VarioSurg — NAKANISHI INC.
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 II | Pending data |
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Manufacturer
- Manufacturer
- Nakanishi Inc.
Sources (1)
- FDA UDI 690efc46-0276-4919-bf6f-aa8910a94df1 33 fields · synced May 30, 2026