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Sterling

FDA UDI

Class II (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
STERLING FDA UDI
Generic Name
Dental diode laser system FDA UDI
Device Name
HP TIP 300UM FIBER 3W LASER 50 FDA UDI
Model / Reference
5006-057 FDA UDI
Description
HP TIP 300UM FIBER 3W LASER 50 FDA UDI

Identifiers

Primary DI / UDI-DI
00366975012906 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental diode laser system

Sterling by Benco Dental Supply Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental diode laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fbf84033-ba82-4728-8974-9c90437beb63 35 fields · synced May 30, 2026