Atlas FDA

TENEO 317 Model 2

FDA premarket approval P990027/S023 · decided 2025-02-04

Approval details

PMA number
P990027
Supplement
S023
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
TENEO 317 Model 2
Generic name
Excimer laser system
Applicant
Technolas Perfect Vision GmbH
Date received
2024-09-30
Decision date
2025-02-04
Days to decision
127 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
München
Statement
Approval for revision of the maximum gas fine filling time in the firmware for the Laser Head

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510(k) clearances by this applicant

RecordFirmDate
VICTUS Femtosecond Laser Platform (K200724)Technolas Perfect Vision GmbH2020-09-01
VICTUS Femtosecond Laser Platform (K171014)Technolas Perfect Vision GmbH2017-10-19
VICTUS Femtosecond Laser Platform (K151161)Technolas Perfect Vision GmbH2015-06-24
VICTUS FEMTOSECOND LASER PLATFORM (K141379)Technolas Perfect Vision GmbH2015-01-16
VICTUS FEMTOSECOND LASER PLATFORM (K140615)Technolas Perfect Vision GmbH2014-07-15
VICTUS FEMTOSECOND LASER PLATFORM (K132534)Technolas Perfect Vision GmbH2014-02-14
VICTUS FEMTOSECOND LASER PLATFORM (K122386)Technolas Perfect Vision GmbH2013-02-08
VICTUS LASER PLATFORM (K120426)Technolas Perfect Vision GmbH2012-07-31