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Posterior CleanFlow Procedure Instrument with Matrix
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Posterior CleanFlow Procedure Instrument with Matrix FDA UDI
- Generic Name
- Dental delivery system instrument unit, electric FDA UDI
- Device Name
- CleanFlow Device used with the GentleWave System to treat root canals (Posterior teeth). FDA UDI
- Model / Reference
- FG-013-00004 FDA UDI
- Description
- CleanFlow Device used with the GentleWave System to treat root canals (Posterior teeth). FDA UDI
Identifiers
- Catalog Number
- GW-PST-PI01 FDA UDI
- Primary DI / UDI-DI
- 00858395006783 FDA UDI
- FDA Product Code
- ELC FDA UDI
- GMDN Term
- Dental delivery system instrument unit, electric 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental delivery system instrument unit, electric
Posterior CleanFlow Procedure Instrument with Matrix by Sonendo, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Sonendo, Inc.
Sources (1)
- FDA UDI 05c986a3-46bc-46d5-9d6f-3f748d24134d 36 fields · synced May 30, 2026