← Back to catalogue

Spacer tip, handpiece

FDA UDI

Class II (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
Spacer tip, handpiece FDA UDI
Generic Name
Dermatological solid-state laser system FDA UDI
Device Name
Spacer tip, handpiece FDA UDI
Model / Reference
130-7012-324 FDA UDI
Description
Spacer tip, handpiece FDA UDI

Identifiers

Primary DI / UDI-DI
00841494100551 FDA UDI
510(k) Number
K121346 FDA UDI
K133364 FDA UDI
K140719 FDA UDI
K143105 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dermatological solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermatological solid-state laser system

Spacer tip, handpiece by Cynosure, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological solid-state laser system.

Cleared under the same submission

K121346 also covers:

K133364 also covers:

K140719 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
Cynosure, LLC

Sources (1)

  • FDA UDI 29677978-f009-456b-acec-d6c1bffb1e98 34 fields · synced Jun 1, 2026