← Back to catalogue

Waterlase iPlus Laser System

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 7200854-209

by Biolase Mg Llc

Identity

Trade Name
Waterlase iPlus Laser System EUDAMED
Waterlase iPlus Dental Laser System FDA UDI
Generic Name
Dental solid-state laser system FDA UDI
Device Name
Waterlase iPlus YSGG all tissue dental laser system, premier, platinum EUDAMED
An all-tissue dental laser system intended for a variety of soft-tissue and hard-tissue procedures. The system includes a laser console with a touch screen control panel/user interface, a delivery system comprising of a fiber optic cable, two handpieces and laser tips, a wired footswitch, and other accessories (protective eyewear, power cords, tip cleaning kit, tip holder). The patient-contacting components of the delivery system require sterilization prior to use. FDA UDI
Model / Reference
7200854-209 EUDAMED
All tissue YSGG dental laser system, platinum, premier FDA UDI
Description
An all-tissue dental laser system intended for a variety of soft-tissue and hard-tissue procedures. The system includes a laser console with a touch screen control panel/user interface, a delivery system comprising of a fiber optic cable, two handpieces and laser tips, a wired footswitch, and other accessories (protective eyewear, power cords, tip cleaning kit, tip holder). The patient-contacting components of the delivery system require sterilization prior to use. FDA UDI

Identifiers

Catalog Number
7200854-209 FDA UDI
Primary DI / UDI-DI
00647529004401 EUDAMEDFDA UDI
Basic UDI-DI
B-00647529004401 EUDAMED
510(k) Number
K210183 FDA UDI
FDA Product Code
GEX FDA UDI
EMDN Code
Z12011014 ERBIUM SURGICAL LASER EUDAMED
GMDN Term
Dental solid-state laser system FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Waterlase iPlus Laser System by Biolase Mg Llc — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biolase Mg Llc
EUDAMED SRN
US-MF-000028587
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED c3249f78-69d6-4fdc-b29a-9d47f73542e3 61 fields · synced Jul 22, 2026
  • FDA UDI 96fad3cc-6b2f-4163-a85d-0a7141fd294f 37 fields · synced May 30, 2026