International Medical Devices Database

Manufacturer Address
Wavelight AG, Industriegebiet Doellnitz 5, Pressath Germany
Source
USFDA
1 Event
- Recall of WaveLight FS 200 Femtosecond Laser System

One device in the database

WaveLight FS 200 Femtosecond Laser System

Model / Serial
Alcon Product Code 8065990714 WaveLight Model 1025 Software Version: Version Blue, Service Pack 2
Product Classification
Ophthalmic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution - USA including states of TX, KS, NC, CA, FL, OH, SC, MD, VA and NY and countries of Switzerland, Germany, Greece, United Kingdom, Ireland, Spain, Italy, Australia, India, Malaysia, France, Finland, Saudi Arabia, Czech Republic, Poland, China and South Korea and Iran.
Product Description
WaveLight FS200 Femtosecond Laser System || Alcon Product Code 8065990714 WaveLight Model 1025 Software Version: Version Blue, Service Pack 2. || The WaveLight FS 200 Laser System is an ophthalmic surgical laser indicated for use in refractive surgery for LASIK flap cutting, lamellar and perforating keratoplasty, and intrastromal surgery for implants.

2 manufacturers with a similar name

Learn more about the data here

WaveLight AG

Manufacturer Parent Company (2017)
Novartis Ag
Source
SATP

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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Wavelight AG

One device in the database

WaveLight FS 200 Femtosecond Laser System

2 manufacturers with a similar name

Wavelight AG

WaveLight AG