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Percussor

FDA UDI

Class I (US FDA UDI)

by Erchonia Corporation

Identity

Trade Name
Percussor FDA UDI
Generic Name
Circulatory/musculoskeletal vibration therapy unit, platform FDA UDI
Device Name
THERAPEUTIC – Handheld Galvanic Massager – IFU temporary reduction of the appearance of cellulite FDA UDI
Model / Reference
VP3 FDA UDI
Description
THERAPEUTIC – Handheld Galvanic Massager – IFU temporary reduction of the appearance of cellulite FDA UDI

Identifiers

Catalog Number
VP3 FDA UDI
Primary DI / UDI-DI
00858985006162 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Circulatory/musculoskeletal vibration therapy unit, platform FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Circulatory/musculoskeletal vibration therapy unit, platform

Percussor by Erchonia Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Circulatory/musculoskeletal vibration therapy unit, platform.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Erchonia Corporation

Sources (1)

  • FDA UDI 3cb5e6b3-b219-4420-bc89-a579014cdbac 34 fields · synced Jun 9, 2026