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Sonoca 300

FDA UDI

Class II (US FDA UDI)

by Söring GmbH

Identity

Trade Name
SONOCA 300 FDA UDI
Generic Name
Ultrasonic surgical system generator FDA UDI
Device Name
Ultrasonic generator, 115V FDA UDI
Model / Reference
15-000B-FL FDA UDI
Description
Ultrasonic generator, 115V FDA UDI

Identifiers

Primary DI / UDI-DI
04250321532667 FDA UDI
510(k) Number
K992026 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
Ultrasonic surgical system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

Yes

FDA UDI

Category: Ultrasonic surgical system generator

Sonoca 300 by Söring GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic surgical system generator.

Cleared under the same submission

K992026 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Söring GmbH

Sources (1)

  • FDA UDI d58f59a3-56d5-4f98-81f4-4af080c6ec76 35 fields · synced May 30, 2026