Identity
- Trade Name
- PDT, Inc. FDA UDI
- Generic Name
- Periodontal curette FDA UDI
- Device Name
- R434 - The PDT Slade Blade™ 3 is designed for the Posterior Narrow with a serrated cutting edge on both ends. For the efficient removal of granulation tissue post extraction, 2.8mm blade. Designed with periodontist Dr. Scott Froum. The Slade Blade™ allows for more efficient removal of granulation tissue in post-extraction sockets because of a unique serrated edge and high-quality steel blade. Thorough removal of cystic infected tissue to leave a clean socket is crucial when preparing to place an implant. PDT’s Slade Blade™ line gives periodontists a more precise blade, sized more accurately for sockets. This allows for cleaner extractions and more effective implant placements. FDA UDI
- Model / Reference
- R434 Slade Blade 3, Posterior Narrow FDA UDI
- Description
- R434 - The PDT Slade Blade™ 3 is designed for the Posterior Narrow with a serrated cutting edge on both ends. For the efficient removal of granulation tissue post extraction, 2.8mm blade. Designed with periodontist Dr. Scott Froum. The Slade Blade™ allows for more efficient removal of granulation tissue in post-extraction sockets because of a unique serrated edge and high-quality steel blade. Thorough removal of cystic infected tissue to leave a clean socket is crucial when preparing to place an implant. PDT’s Slade Blade™ line gives periodontists a more precise blade, sized more accurately for sockets. This allows for cleaner extractions and more effective implant placements. FDA UDI
Identifiers
- Catalog Number
- R434 FDA UDI
- Primary DI / UDI-DI
- 00813677022035 FDA UDI
- FDA Product Code
- EMK FDA UDI
- GMDN Term
- Periodontal curette 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Periodontal curette
PDT, Inc. by PDT, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- PDT, Inc.
Sources (1)
- FDA UDI 0c90efdf-6b06-4474-bcb2-30ff15ed5faa 34 fields · synced Jun 9, 2026