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NeuroSITE

FDA UDI

Class II (US FDA UDI)

by Neuronetics Inc.

Identity

Trade Name
NeuroSITE FDA UDI
Generic Name
Magnetic neural stimulation system FDA UDI
Device Name
The NeuroSITE is used to aid in the process of determining and recording the coil locations during the motor threshold (MT) and treatment processes. FDA UDI
Model / Reference
81-72024-000 FDA UDI
Description
The NeuroSITE is used to aid in the process of determining and recording the coil locations during the motor threshold (MT) and treatment processes. FDA UDI

Identifiers

Primary DI / UDI-DI
00850005944300 FDA UDI
510(k) Number
K233621 FDA UDI
FDA Product Code
QCI FDA UDI
OBP FDA UDI
GMDN Term
Magnetic neural stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5802 FDA UDI
882.5805 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

Yes

FDA UDI

Category: Magnetic neural stimulation system

NeuroSITE by Neuronetics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic neural stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neuronetics Inc.

Sources (1)

  • FDA UDI e34a04d0-ebae-427e-8393-1f1cb209557f 35 fields · synced May 30, 2026