Atlas FDA

PureVision (balafilcon A) Contact Lens

FDA premarket approval P980006/S032 · decided 2021-08-27

Approval details

PMA number
P980006
Supplement
S032
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
PureVision (balafilcon A) Contact Lens
Generic name
Lenses, soft contact, extended wear
Applicant
Bausch & Lomb, Inc.
Date received
2021-06-03
Decision date
2021-08-27
Days to decision
85 days
Decision code
APPR
Product code
LPM
Advisory committee
Ophthalmic
Expedited review
No
Location
Rochester, NY
Statement
Approval to remove the Sagittal Depth measurement acceptance criteria from the finished product specifications for PureVision (balafilcon A) Contact Lens.

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510(k) clearances by this applicant

RecordFirmDate
Bausch + Lomb PreVue Inserter for enVista Preloaded (K192005)Bausch & Lomb, Inc.2019-10-04
Crystalsert Lens Delivery System (K173480)Bausch & Lomb, Inc.2017-12-11
Bausch + Lomb Injector System (K151102)Bausch & Lomb, Inc.2015-05-22
BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA, (K131208)Bausch & Lomb, Inc.2013-09-11
BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VI (K122575)Bausch & Lomb, Inc.2012-12-20
BAUSCH & LOMB IOL INJECTOR (K113852)Bausch & Lomb, Inc.2012-09-28
OCD04 3% HYDROGEN PEROXIDE CLEANING AND DISINFECTING SOULTION (K112909)Bausch & Lomb, Inc.2012-04-30
EZS05 CLEANING AND DISINFECTING SOLUTION, BAUSCH + LOMB EZS05 CLEANING AND DISINFECTING SOLUTION (K111877)Bausch & Lomb, Inc.2012-01-24