Intra Lase Corp.
United StatesFDA applicant, unverified
- Devices
- 9
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Intralase Fs Laser Ref K041893
Regimes: 510(k) Registry: 510(k)Modification To Intralase 600C Laser Keratome Ref K001211
Regimes: 510(k) Registry: 510(k)Ifs Laser System Ref K073404
Regimes: 510(k) Registry: 510(k)Intralase Fs Laser Ref K031960
Regimes: 510(k) Registry: 510(k)Pulsion Fs Laser Keratome Ref K013941
Regimes: 510(k) Registry: 510(k)Intralase 600C Laser Keratome Ref K002890
Regimes: 510(k) Registry: 510(k)Intralase Fusion Laser Ref K063682
Regimes: 510(k) Registry: 510(k)Intralase 600C Laser Keratome Ref K993153
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
FDA recalls
2003
- 15 Jul 2003 Z-1124-03 Unclassified (pre-2012) Terminated Gantry moves toward patient when 'Home' button is used after procedure.
Frequently asked questions
How many devices does Intra Lase Corp. have in the registry?
The registry currently lists 9 devices for Intra Lase Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intra Lase Corp.'s devices?
Among its 9 most recently registered devices, Intra Lase Corp. has devices listed in FDA 510(k) (9 devices).
What risk classes do Intra Lase Corp.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Intra Lase Corp.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Intra Lase Corp.?
FDA recall records list 1 recall initiated by Intra Lase Corp., the most recent initiated on 15 Jul 2003. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Intra Lase Corp. in the registry?
The most recently registered devices listed for Intra Lase Corp. include INTRALASE FS LASER, MODIFICATION TO INTRALASE 600C LASER KERATOME, IFS LASER SYSTEM and PULSION FS LASER KERATOME.