Identity
- Trade Name
- HybenX FDA UDI
- Generic Name
- Root canal cleaning solution FDA UDI
- Device Name
- HybenX OTD Syringe (2-Pack) FDA UDI
- Model / Reference
- 103-2001 FDA UDI
- Description
- HybenX OTD Syringe (2-Pack) FDA UDI
Identifiers
- Catalog Number
- 103-2001 FDA UDI
- Primary DI / UDI-DI
- 00813110027337 FDA UDI
- 510(k) Number
- K123538 FDA UDI
- FDA Product Code
- KJJ FDA UDI
- GMDN Term
- Root canal cleaning solution FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Root canal cleaning solution
HybenX by Bicon, Llc — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Bicon, Llc
Sources (1)
- FDA UDI c7b3a5eb-4435-4692-a1ea-9938aaf05523 36 fields · synced May 30, 2026