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Trophy Skin

FDA UDI

Class II (US FDA UDI)

by Trophy Skin, Inc.

Identity

Trade Name
Trophy Skin FDA UDI
Generic Name
Hand-held deep-tissue electromagnetic stimulator FDA UDI
Device Name
RejuvatoneMD Facial Toning Device FDA UDI
Model / Reference
REJUVATONEMD FDA UDI
Description
RejuvatoneMD Facial Toning Device FDA UDI

Identifiers

Primary DI / UDI-DI
00851561006105 FDA UDI
510(k) Number
K152199 FDA UDI
FDA Product Code
NFO FDA UDI
GMDN Term
Hand-held deep-tissue electromagnetic stimulator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand-held deep-tissue electromagnetic stimulator

Trophy Skin by Trophy Skin, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held deep-tissue electromagnetic stimulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trophy Skin, Inc.

Sources (1)

  • FDA UDI b0f50c58-ec18-41f5-a8d4-a98d9f3a2ab7 35 fields · synced May 30, 2026