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Manufacturer profile

Cutera, Inc.

EU EUDAMEDUnited States16 registered devices
VerifiedEUDAMED · official EU database
16
Total devices
1
Risk classes
2024
Earliest version
2024
Latest version
Regulatory footprint
Search Cutera, Inc. across other regulatory registries
ThailandColombiaSouth KoreaCanadaEcuadorSaudi Arabia
Recent products (latest 10)
Most recently updated devices in the database
enlighten III
00816722021649
Class IIb
enlighten SR
00816722021625
Class IIb
excel HR
00816722021502
Class IIb
excel V+
00816722021311
Class IIb
xeo
00816722021106
Class IIb
xeo SA
00816722021113
Class IIb
AcuTip 500
00816722022103
Class IIb
Limelight
00816722022110
Class IIb
ProWave LX
00816722022134
Class IIb
Pearl Fractional
00816722022158
Class IIb
Risk class distribution
Breakdown by risk classification
Class IIb16100.0% of total
Top authorized representatives
Most common authorized representatives for this manufacturer
MDSS GmbH
100.0%16 devices
About this profile

Explore comprehensive manufacturer profile for Cutera, Inc. through Pure Global AI's free EU medical device database. This company manufactures 16 medical devices registered with EUDAMED across 1 risk class based in United States.

This page provides detailed insights including recent registrations, risk class distribution (Class IIb: 16), and complete regulatory information from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry.