Atlas FDA

Boston Orthokeratology (oprifocon A) Shaping lens for Overnight Wear for Bausch + Lomb Vision Shaping Treatment

FDA premarket approval P010062/S014 · decided 2025-02-20

Approval details

PMA number
P010062
Supplement
S014
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Boston Orthokeratology (oprifocon A) Shaping lens for Overnight Wear for Bausch + Lomb Vision Shaping Treatment
Generic name
Lens, contact, orthokeratology, overnight
Applicant
Bausch & Lomb
Date received
2024-11-22
Decision date
2025-02-20
Days to decision
90 days
Decision code
APPR
Product code
NUU
Advisory committee
Ophthalmic
Expedited review
No
Location
Rochester, NY
Statement
implementing a design module of the existing software for generating lathe cutting files to provide alternative posterior lens designs for Boston Orthokeratology (oprifocon A) Shaping Lens for Overnight Wear for Bausch + Lomb Vision Shaping Treatment

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510(k) clearances by this applicant

RecordFirmDate
Stellaris Elite vision enhancement system (K170052)Bausch+Lomb2017-04-19
Stellaris Elite Vision Enhancement System (K162342)Bausch+Lomb2017-03-24
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STELLARIS VISION ENHANCEMENT SYSTEM (K133242)Bausch & Lomb2014-02-14
BAUSCH & LOMB INJECTOR SYSTEM (K131958)Bausch & Lomb2014-01-09
BAUSCH + LUMB, VIS100 INJECTOR SYSTEM (K133146)Bausch & Lomb2014-01-03
EASY-LOAD LENS DELIVERY SYSTEM (K132481)Bausch & Lomb2013-12-27
CRYSTALSERT DELIVERY SYSTEM (K132593)Bausch & Lomb2013-09-17