Identity
- Trade Name
- No Mix30 FDA UDI
- Generic Name
- Orthodontic bracket adhesive FDA UDI
- Device Name
- NO MIX:30 ADHESIVE SYRINGE KIT FDA UDI
- Model / Reference
- 001-910 FDA UDI
- Description
- NO MIX:30 ADHESIVE SYRINGE KIT FDA UDI
Identifiers
- Catalog Number
- 001-910 FDA UDI
- Primary DI / UDI-DI
- 00190746007767 FDA UDI
- 510(k) Number
- K893037 FDA UDI
- FDA Product Code
- DYH FDA UDI
- GMDN Term
- Orthodontic bracket adhesive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3750 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
Yes
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: Orthodontic bracket adhesive
No Mix30 by American Orthodontics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K893037 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- American Orthodontics
Sources (1)
- FDA UDI d5ba8517-32a1-4ec4-968f-f04e0d3f384e 37 fields · synced Jun 9, 2026