← Back to catalogue

SonicOne Clinic

FDA UDI

Class U (US FDA UDI)

by Misonix, LLC

Identity

Trade Name
SonicOne Clinic FDA UDI
Generic Name
Soft-tissue ultrasonic surgical system handpiece tip, single-use FDA UDI
Device Name
SonicOne Clinic Blue Cyclindrical Titanium Probe Kit (w/Wrench) FDA UDI
Model / Reference
E-SOP-R1 FDA UDI
Description
SonicOne Clinic Blue Cyclindrical Titanium Probe Kit (w/Wrench) FDA UDI

Identifiers

Primary DI / UDI-DI
00841626101005 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Soft-tissue ultrasonic surgical system handpiece tip, single-use FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Soft-tissue ultrasonic surgical system handpiece tip, single-use

SonicOne Clinic by Misonix, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue ultrasonic surgical system handpiece tip, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Misonix, LLC

Sources (1)

  • FDA UDI 0fbfd65d-6dce-4607-9f0a-62784770919b 33 fields · synced Jun 9, 2026