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DENZA I-Tip

FDA UDI

Class II (US FDA UDI)

by Jeisys Medical Inc.

Identity

Trade Name
DENZA I-Tip FDA UDI
Generic Name
Radio-frequency skin/body contouring system FDA UDI
Device Name
DENZA I-Tip FDA UDI
Model / Reference
DENZA I-Tip FDA UDI
Description
DENZA I-Tip FDA UDI

Identifiers

Primary DI / UDI-DI
08800020103963 FDA UDI
510(k) Number
K230663 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Radio-frequency skin/body contouring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radio-frequency skin/body contouring system

DENZA I-Tip by Jeisys Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin/body contouring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jeisys Medical Inc.

Sources (1)

  • FDA UDI ec870628-6c76-4e8f-afa4-edeb25f72d1d 34 fields · synced Jun 1, 2026