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VarioSurg

FDA UDI

Class II (US FDA UDI)

by Nakanishi Inc.

Identity

Trade Name
VarioSurg FDA UDI
Generic Name
Dental ultrasonic surgical system generator FDA UDI
Model / Reference
VarioSurg Unit FDA UDI

Identifiers

Primary DI / UDI-DI
04560264508385 FDA UDI
510(k) Number
K073678 FDA UDI
FDA Product Code
DZI FDA UDI
ELC FDA UDI
GMDN Term
Dental ultrasonic surgical system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 FDA UDI
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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental ultrasonic surgical system generator

VarioSurg by Nakanishi Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental ultrasonic surgical system generator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nakanishi Inc.

Sources (1)

  • FDA UDI d35879a5-65c7-47a2-b7a0-0a3505f6f6cb 33 fields · synced May 30, 2026