Atlas FDA

iDESIGN Refractive Studio

FDA premarket approval P930016/S061 · decided 2020-02-14

Approval details

PMA number
P930016
Supplement
S061
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
iDESIGN Refractive Studio
Generic name
Excimer laser system
Applicant
Amo Manufacturing USA, LLC
Date received
2019-11-25
Decision date
2020-02-14
Days to decision
81 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
Milpitas, CA
Statement
Approval for a replacement of a Super Luminescent Diode (SLD) used in the iDESIGN Refractive Studio as a replacement for an SLD that is now obsolete.

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510(k) clearances by this applicant

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Catalys™ Precision Laser System (K223838)Amo Manufacturing USA, LLC2023-04-12
CATALYS Precision Laser system (K220516)Amo Manufacturing USA, LLC2022-05-17
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Catalys Precision Laser System (K182083)Amo Manufacturing USA, LLC2018-11-09
Catalys Precision Laser System (K172002)Amo Manufacturing USA, LLC2017-08-25
IFS ADVANCED FEMTOSECOND LASER SYSTEM (K141852)Amo Manufacturing USA, LLC2015-01-06