AcuTip 500

GUDID 00816722022103

AcuTip 500 IPL Handpiece

CUTERA, INC.

Laser skin surface treatment system applicator
Primary Device ID00816722022103
NIH Device Record Keye99735e7-3779-466e-b4db-b7484c569c89
Commercial Distribution StatusIn Commercial Distribution
Brand NameAcuTip 500
Version Model NumberAcuTip 500
Company DUNS041071643
Company NameCUTERA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100816722022103 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-23

Devices Manufactured by CUTERA, INC.

00816722022806 - Acutip2023-05-23 Acutip IPL Handpiece for xeo+/xeo+ SA
00816722021809 - xeo+2022-12-08 xeo+ Laser System
00816722021816 - xeo+ SA2022-12-08 xeo+ SA IPL System
00816722022813 - Limelight 2022-12-08 Limelight IPL Handpiece for xeo+/xeo+ SA
00816722022820 - Prowave 2022-12-08 Prowave IPL Handpiece for xeo+/xeo+ SA
00816722022837 - Titan2022-12-08 Titan IPL Handpiece for xeo+/xeo+ SA
00816722022844 - Pearl Fractional2022-12-08 Pearl Fractional Laser Handpiece for xeo+/xeo+ SA
00816722022479 - truSculpt 2 RF handpiece2022-11-22 truSculpt 2 cm^2 handheld handpiece for use with truSculpt iD RF device

Trademark Results [AcuTip 500]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ACUTIP 500
ACUTIP 500
78670925 3199758 Live/Registered
Cutera, Inc.
2005-07-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.