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Hu-Friedy

FDA UDI

Class II (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
Hu-Friedy FDA UDI
Generic Name
Ultrasonic dental scaling/debridement system generator FDA UDI
Device Name
Symmetry IQ 2000 Lux Handpiece Cord FDA UDI
Model / Reference
UP2HPLC FDA UDI
Description
Symmetry IQ 2000 Lux Handpiece Cord FDA UDI

Identifiers

Catalog Number
UP2HPLC FDA UDI
Primary DI / UDI-DI
10889950002497 FDA UDI
510(k) Number
K070975 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Ultrasonic dental scaling/debridement system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ultrasonic dental scaling/debridement system generator

Hu-Friedy by Hu-Friedy Mfg Co., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic dental scaling/debridement system generator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 75cfc375-f3b0-463e-9a3d-63f4f89a364f 36 fields · synced May 30, 2026