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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Reflective dental room light FDA UDI
Device Name
Light Splash Shield for Ritter/Marus FDA UDI
Model / Reference
LSS-602 FDA UDI
Description
Light Splash Shield for Ritter/Marus FDA UDI

Identifiers

Catalog Number
LSS-602 FDA UDI
Primary DI / UDI-DI
D832LSS6020 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Reflective dental room light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

Category: Reflective dental room light

Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reflective dental room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 1d372954-1524-462e-943f-f3f061a44b18 34 fields · synced May 30, 2026