← Back to catalogue

Forma

FDA UDI

Class II (US FDA UDI)

by Inmode MD , Ltd.

Identity

Trade Name
Forma FDA UDI
Generic Name
Radio-frequency skin surface treatment system applicator FDA UDI
Device Name
Forma (i.e. Firm-Forma 4 elec) FDA UDI
Model / Reference
AG603799A FDA UDI
Description
Forma (i.e. Firm-Forma 4 elec) FDA UDI

Identifiers

Catalog Number
AG603799A FDA UDI
Primary DI / UDI-DI
07290016633061 FDA UDI
510(k) Number
K140926 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Radio-frequency skin surface treatment system applicator 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

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

Yes

FDA UDI

Category: Radio-frequency skin surface treatment system applicator

Forma by Inmode MD , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin surface treatment system applicator.

Cleared under the same submission

K140926 also covers:

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
Inmode MD , Ltd.

Sources (1)

  • FDA UDI f8059cf2-bd32-4c0e-b87f-a37a0eead9cf 37 fields · synced May 30, 2026