Identity
- Trade Name
- Diode Laser Tips FDA UDI
- Generic Name
- Dental diode laser system FDA UDI
- Device Name
- A single-use fiberoptic pre-initiated tip intended for use with Epic Pro Diode Laser Systems. FDA UDI
- Model / Reference
- PI Pro Tips, Surgical, 4-4 FDA UDI
- Description
- A single-use fiberoptic pre-initiated tip intended for use with Epic Pro Diode Laser Systems. FDA UDI
Identifiers
- Catalog Number
- 7430002 FDA UDI
- Primary DI / UDI-DI
- 00647529003183 FDA UDI
- 510(k) Number
- K163128 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Dental diode laser system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 400 Micrometer FDA UDILength — 4 Millimeter FDA UDI
Category: Dental diode laser system
Diode Laser Tips by Biolase, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental diode laser system.
- NV®PRO3 — Den-Mat Holdings, LLC · Class II
- NV® — Den-Mat Holdings, LLC · Class II
- Dental Diode Laser System — Lazon Medical Laser Co., Ltd. · Class II
- STERLING® — Den-Mat Holdings, LLC · Class II
- SOL® — Den-Mat Holdings, LLC · Class II
- BLU — Peter Brasseler Holdings, LLC · Class II
- Pioneer Elite Perio Tip — CAO GROUP, INC. · Class II
- SL3® — Den-Mat Holdings, LLC · Class II
Cleared under the same submission
K163128 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
- Biolase, Inc.
Sources (1)
- FDA UDI bfb7c4a0-1126-4cf0-b34b-1662e1868ceb 37 fields · synced Jun 8, 2026