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Sting Doctor

FDA UDI

Class II (US FDA UDI)

by Spark Innovators Corporation

Identity

Trade Name
Sting Doctor FDA UDI
Generic Name
Insect bite/sting hyperthermia device FDA UDI
Device Name
The Sting Doctor is a handheld, battery powered device that uses targeted heat therapy intended to help reduce the itch and irritation caused by insect bites/stings from mosquitoes, bees, and wasps. FDA UDI
Model / Reference
SD-MC6 FDA UDI
Description
The Sting Doctor is a handheld, battery powered device that uses targeted heat therapy intended to help reduce the itch and irritation caused by insect bites/stings from mosquitoes, bees, and wasps. FDA UDI

Identifiers

Primary DI / UDI-DI
00850018026109 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Insect bite/sting hyperthermia device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5740 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Insect bite/sting hyperthermia device

Sting Doctor by Spark Innovators Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insect bite/sting hyperthermia device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2eeb62e6-b735-44d6-8717-3dfc0f301714 34 fields · synced May 31, 2026