Identity
- Trade Name
- PIEZON FDA UDI
- Generic Name
- Ultrasonic dental scaling/debridement system handpiece tip, periodontal FDA UDI
- Device Name
- Instrument A x3 FDA UDI
- Model / Reference
- DS-001A/T FDA UDI
- Description
- Instrument A x3 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07613353179557 FDA UDI
- 510(k) Number
- K093000 FDA UDI
- FDA Product Code
- ELC FDA UDI
- GMDN Term
- Ultrasonic dental scaling/debridement system handpiece tip, periodontal FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.4850 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ultrasonic dental scaling/debridement system handpiece tip, periodontal
Piezon by E.M.S. Electro Medical Systems S.A. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K093000 also covers:
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
- PIEZON — E.M.S. Electro Medical Systems S.A.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- E.M.S. Electro Medical Systems S.A.
Sources (1)
- FDA UDI 28dfd170-c15c-47e4-9baf-25408f2a2db6 35 fields · synced May 30, 2026