Clarteis

FDA Filings

This page includes the latest FDA filings for Clarteis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3014226003
• FEI Number: 3014226003
• Name: CLARTEIS
• Owner & Operator: CLARTEIS
• Contact Address: WTC2, 120 route des macarons ; Valbonne FR-06 Alpes-Maritimes 06560 FR
• Official Correspondent:
  • Laurent MEILHAC
  • 33-6-0999044-x
• US Agent:
  • Allison Komiyama
  • Acknowledge
  • 619 2087888
  • akomiyama@acknowledge-rs.com
• Importing Logistics Registration:
  • Importer: Excimer Therapies Inc.
  • Address: 6440 Lusk Blvd, Suite D206 ; San Diego, CA 92121 UNITED STATES
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: WTC2, 120 route des macarons ; Valbonne Alpes-Maritimes, 06560 FR
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 03760313461017 CLARTEIS	EXCI308 by Aerolase EIPL-PRD-K01-exci308	2022-06-21
GUDID 03760313461000 CLARTEIS	Exciplex® EIPL-PRD-K01-(US)	2020-09-17
PMN K191086 Clarteis	Exciplex	2019-12-11
PMN K171702 | GEX CLARTEIS	Exciplex 308nm	2018-02-05
PMN K171702 | FTC CLARTEIS	Exciplex 308nm	2018-02-05
PMN K171702 Clarteis	Exciplex308nm	2017-10-13