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Diode Laser Tips

FDA UDI

Class II (US FDA UDI)

by Biolase, Inc.

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 diode laser systems. FDA UDI
Model / Reference
Pre-initiated, Surgical, 3-4 FDA UDI
Description
A single-use fiberoptic pre-initiated tip intended for use with diode laser systems. FDA UDI

Identifiers

Catalog Number
7400071 FDA UDI
Primary DI / UDI-DI
00647529003343 FDA UDI
510(k) Number
K121286 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 300 Micrometer FDA UDI
Length — 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biolase, Inc.

Sources (1)

  • FDA UDI cbee8949-9bee-4e90-99b5-8ea7970f32a2 37 fields · synced May 31, 2026