Identity
- Trade Name
- BEYOND® FlexiPro™ Cheek Retractor (single pack)-M FDA UDI
- Generic Name
- Dental cheek retractor, professional, single-use FDA UDI
- Model / Reference
- BY-M016-M FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00857848007698 FDA UDI
- FDA Product Code
- EIG FDA UDI
- GMDN Term
- Dental cheek retractor, professional, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental cheek retractor, professional, single-use
BEYOND® FlexiPro™ Cheek Retractor (single pack)-M by Beyond International Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental cheek retractor, professional, single-use.
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- Cheek Retractor — DR.FRIGZ INTERNATIONAL(PVT)LTD, · Class I
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- Denovo Clearfield cheek retractors — DENOVO DENTAL INC · Class I
- Geistlich Panorama — DSSM AG · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Beyond International Inc.
Sources (1)
- FDA UDI bdb04e48-66fc-4b09-9313-8effc62e942a 32 fields · synced Jun 9, 2026