Philips Zoom

FDA UDI

Class I (US FDA UDI)

by Discus Dental, Inc.

Identity

Trade Name: Philips Zoom FDA UDI
Generic Name: Tooth-bleaching acceleration unit FDA UDI
Device Name: Zoom! Lamp upgrade Head FDA UDI
Model / Reference: DIS578/01 FDA UDI
Description: Zoom! Lamp upgrade Head FDA UDI

Identifiers

Primary DI / UDI-DI: 08710103632122 FDA UDI
FDA Product Code: KPY FDA UDI
EEG FDA UDI
IWS FDA UDI
GMDN Term: Tooth-bleaching acceleration unit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 892.6500 FDA UDI
872.6475 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Tooth-bleaching acceleration unit

Philips Zoom by Discus Dental, 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: Discus Dental, Inc.

Sources (1)

FDA UDI 52027140-5340-425e-b101-8e6069727f0b 33 fields · synced May 30, 2026