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ASSY, Face Accessory Kit, TempSure

FDA UDI

Class II (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
ASSY, Face Accessory Kit, TempSure FDA UDI
Generic Name
Electrosurgical system FDA UDI
Device Name
ASSY, Face Accessory Kit, TempSure FDA UDI
Model / Reference
100-7027-065 FDA UDI
Description
ASSY, Face Accessory Kit, TempSure FDA UDI

Identifiers

Primary DI / UDI-DI
00841494107673 FDA UDI
510(k) Number
K171262 FDA UDI
FDA Product Code
GEI FDA UDI
PBX FDA UDI
GMDN Term
Electrosurgical 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical system

ASSY, Face Accessory Kit, TempSure by Cynosure, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI 5f2bd687-574e-465a-9bc4-d1fd04642b22 34 fields · synced May 30, 2026