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Dentech

FDA UDI

Class I (US FDA UDI)

by Dentech Corp.

Identity

Trade Name
DENTECH FDA UDI
Generic Name
LED dental light, battery-powered FDA UDI
Model / Reference
30080350 FDA UDI

Identifiers

Primary DI / UDI-DI
04560218680945 FDA UDI
FDA Product Code
EAY FDA UDI
GMDN Term
LED dental light, battery-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4620 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

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

Category: LED dental light, battery-powered

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

Similar devices

Also classified as LED dental light, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentech Corp.

Sources (1)

  • FDA UDI a8184c17-fa8a-4ccf-b3bf-e0dd946f65f6 32 fields · synced May 30, 2026