Identity
- Trade Name
- BlueCheck FDA UDI
- Generic Name
- Dental caries detecting stain FDA UDI
- Device Name
- BlueCheck Caries Detection & Monitoring Medical Device Dental 0.3 mL x 1 FDA UDI
- Model / Reference
- BN01AUS FDA UDI
- Description
- BlueCheck Caries Detection & Monitoring Medical Device Dental 0.3 mL x 1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 09359621000021 FDA UDI
- 510(k) Number
- K222560 FDA UDI
- FDA Product Code
- LFC FDA UDI
- GMDN Term
- Dental caries detecting stain FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.1740 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental caries detecting stain
BlueCheck by Incisive Technologies Pty, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K222560 also covers:
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
- Incisive Technologies Pty, Ltd.
Sources (1)
- FDA UDI 01bcd551-71a4-45c5-b3b5-b2ccab31a1da 34 fields · synced May 30, 2026