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Cure Medical

FDA UDI

Class II (US FDA UDI)

by Liger Medical

Identity

Trade Name
Cure Medical FDA UDI
Generic Name
Electrocautery system generator, battery-powered FDA UDI
Device Name
19mm Flat Probe Accessory for the HTU-110. FDA UDI
Model / Reference
HTU-110 19mm Flat FDA UDI
Description
19mm Flat Probe Accessory for the HTU-110. FDA UDI

Identifiers

Primary DI / UDI-DI
00861592000348 FDA UDI
510(k) Number
K152843 FDA UDI
FDA Product Code
HGI FDA UDI
GMDN Term
Electrocautery system generator, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4120 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
MRI Safety
MR Unsafe FDA UDI

Category: Electrocautery system generator, battery-powered

Cure Medical by Liger Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocautery system generator, battery-powered.

Cleared under the same submission

K152843 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Liger Medical

Sources (1)

  • FDA UDI c784a195-378c-4e84-ac53-6954aa9c6236 34 fields · synced Jun 9, 2026