Envista Aspire™ Toric IOL

enVista Aspire toric hydrophobic acrylic IOL (non-preloaded) +13.00D SE / +5.00D CYL

Registry build 21.09.26
1manufacturer
798catalogue numbers in this listing
10recalls on this code

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code HQL
Manufacturer City Province Registered as Device types
Wuxi Vision PRO Ltd Wuxi Jiangsu Manufacturer 1

Record

Regulatory record for enVista Aspire™ Toric IOL
Listed by Bausch & Lomb Incorporated, United States
FDA product code HQL
Device type Intraocular Lens
Device class Class 3
Regulation 21 CFR 886.3600
Establishment Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2023-11-17
Record revised 2024-06-11 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for enVista Aspire™ Toric IOL
Catalogue number Size Status
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Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Clareon Alcon Laboratories, Inc. 1,760
enVista® Toric IOL Bausch & Lomb Incorporated 1,274
AcrySof® Alcon Laboratories, Inc. 1,223
EnVista MX60 IOL Bausch & Lomb Incorporated 1,050
Isotechnics Eyekon Medical, Inc. 1,008
MDR Eyekon Medical, Inc. 1,007
DGR Eyekon Medical, Inc. 1,007
Acuity Eyekon Medical, Inc. 1,007
Acurus Eyekon Medical, Inc. 901
Cirrus Eyekon Medical, Inc. 901
Eyekon Eyekon Medical, Inc. 901
Suncoast Eyekon Medical, Inc. 795

Showing 12 of 71. All products under Intraocular Lens

Recalls

1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2025-06-06 Class III Process control An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in functional visual impairment or reduction in visual acuity which could resul 2
2025-03-27 Class I Process control In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S. 236,840
2020-06-09 Class II Unknown/Undetermined by firm The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens. 5 2021-02-11
2018-11-05 Class II Process control Cosmetic imperfections on the surface of some lenses. 70,440 units 2019-11-04
2015-05-26 Class II Device Design Haptics breaking during lens loading and insertion. 72,773 units; 52,787 units (US) 19,986 units (Foreign) 2016-08-25
2015-05-26 Class II Device Design Haptics breaking during lens loading and insertion. 72,773 units. 52,787 units (US) – 19,986 units (Foreign) 2016-08-25
2013-10-16 Class II Nonconforming Material/Component Lens was manufactured with incorrect raw material. 336 IOLs (283 IOLs in the US, 53 IOLs outside the US) 2014-09-17
2009-11-19 Not classified Other Bausch & Lomb Incorporated, Rochester, NY is recalling their Silicone L161SE Intraocular Lens Lot 4916928 (23.5D) after receiving three customer complaints for what appears to be opacification of the intraocular lens. The opacification occ 85 lenses 2010-07-22
2008-12-08 Not classified Release of Material/Component prior to receiving test results Affected lenses were inadvertently shipped to Bausch & Lomb’s European Logistics Center (ELC) prior to release authorization. Initial testing indicated the product did not meet release criteria for endotoxin limits. 158 2009-11-05
2004-02-27 Not classified Other Lens may be labeled with incorrect diopter size. 36 2012-05-03

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P190018 2026-07-06 Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon Toric Aspheric Hydrophobic Acrylic Intraocular Lens Alcon Laboratories, Inc.
P240038 2025-09-10 FINEVISION HP Trifocal IOLs Beaver-Visitec International, Ltd
P930014 2023-10-24 AcrySof® Posterior Chamber Intraocular Lens and Delivery Systems Alcon Laboratories, Inc.
P100016 2023-01-05 CT LUCIA Intraocular Lens (IOL) Carl Zeiss Meditec Production, LLC.
P060011 2019-04-12 Rayner C-flex 570C, C-flex Aspheric 970C and 600C Aspheric Intraocular lenses Rayner Intraocular Lenses Limited
P060022 2018-08-07 Akreos Intraocular Lens Bausch & Lomb Incorporated
P910056 2012-10-19 EN VISTA HYDROPHOBIC ACRYLIC INTRAOCULAR LENS Bausch & Lomb Incorporated
P090022 2012-09-20 LENSTEC SOFTEC HD PCIOL Lenstec, Inc.
P990080 2012-05-23 TECNIS MULTIFOCAL INTRAOCULAR LENS, MODEL ZMA00 Johnson & Johnson Surgical Vision, Inc.
P880081 2012-04-23 AMO CLARIFLEX INTRAOCULAR LENSES (IOL) ( MODELS CLRFLX/CLRFLXB/CLRFLXC) & TECNIS CL 3-PIECE INTRAOCULAR LENS (IOL) Johnson & Johnson Surgical Vision, Inc.
P080004 2012-01-20 BIOLOGICAL INDICATOR (BI) Hoya Surgical Optics, Inc.
P810032 2011-07-21 ACRYSOF RESTOR INTRAOCULAR LENSES Alcon Laboratories, Inc.
P840060 2010-06-02 PMMA INTRAOCULAR LENSES Alcon Laboratories, Inc.
P010027 2010-03-12 ANTERIOR CHAMBER INTRAOCULAR LENS Aaren Scientific Inc
P080021 2009-02-02 XACT FOLDABLE HYDROPHOBIC ACRYLIC ULTRAVIOLET LIGHT-ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS (IOL) Bausch & Lomb Incorporated
P980040 2007-03-22 AMO SENSAR SOFT ACRYLIC MONOFOCAL INTRAOCULAR LENSES (IOLS) Johnson & Johnson Surgical Vision, Inc.
P990013 2007-03-22 STAAR SURGICAL COLLAMER INTRAOCULAR LENSES Starr Surgical Co.
P880091 2005-10-19 ELASTIC LENS SINGLE-PIECE SILICONE POSTERIOR CHAMBER IOL Staar Surgical Company
P880087 2005-03-04 PMMA SINGLE-PIECE ANTERIOR CHAMBER INTRAOCULAR LENSES Alcon Laboratories, Inc.
P880070 2005-02-04 CEEON HEPARIN SURFACE MODIFIED UV-LIGHT ABSORBING ANTERIOR CHAMBER (IOLS) Abbott Medical Optics, Inc.
P990014 2003-09-16 HYDROVIEW COMPOSITE HYGROGEL FOLDABLE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER INTRAOCULAR (IOL) Bausch & Lomb Incorporated
P910058 2003-08-13 SILICONE INTRAOCULAR LENSES Bausch & Lomb Incorporated
P910061 2003-07-23 BIOBURDEN TESTING Bausch & Lomb Incorporated
P970034 1998-09-25 MODIFIED C-LOOP, UV-ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENSES Aaren Scientific Inc
P800049 1998-09-04 IRIDOCAPSULAR INTRAOCULAR LENS Alcon, Inc.
P960036 1997-12-22 MEMORYLENS ULTRAVIOLET-ABSORBING HYDROPHILIC POSTERIOR CHAMBER INTRAOCULAR LENS (MODEL U940A) Ioltech, S.A.
P890056 1997-10-02 MODEL PC-28LB POSTERIOR CHAMBER INTRAOCULAR LENS Advanced Medical Optics, Inc.
P940007 1996-12-10 PLIOLENS UV ABSORBING SILICONE POST. CHAM. IOL/FOLDABLE IOL MODEL 127(920) Advanced Medical Optics, Inc.
P880072 1996-04-17 MODELS GL65C-OUV ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS (IOL) Eyekon Medical, Inc.
P830056 1996-04-02 POSTERIOR CHAMBER INTROCULAR LENSES Carl Zeiss Meditec Inc
P810055 1994-08-23 CM(TM) LENSES Advanced Medical Optics, Inc.
P910060 1994-04-20 ELASTIMIDE(TM) IOL MODEL AQ-2010 Staar Surgical Company
P840039 1994-03-28 J-LOOP POSTERIOR CHAMBER INTRAOCULAR LENS Bausch & Lomb Incorporated
P900048 1993-08-23 ELASTIMIDE(TM) SILICONE MODIFIED C-LOOP POST. CHAM Staar Surgical Company
P860034 1992-11-09 MODELS AC-21/AC-21B ANTERIOR CHAMBER IOL Advanced Medical Optics, Inc.
P840033 1992-05-29 MODELS KR2V, SK21V, S2BV Alcon Laboratories, Inc.
P820016 1991-12-20 ZIRCONIA SILICATE BEAD IOL TUMBLE POLISHING Cilco, Inc.
P880085 1991-06-27 MODEL 405 SPANFLEX TM IOL Advanced Medical Optics, Inc.
P900037 1991-02-28 MODIFIED J&C LOOP POST. CHAMBER INTRAOCULAR LENS Medical Development Research, Inc.
P900053 1991-02-28 MODELS A21-A & A21-B POSTERIOR CHAMBER INTRAOCULAR Vision Medical Inc
P860002 1990-11-15 COBURN(R) POSTERIOR INTRAOCULAR LENSES Bausch & Lomb Incorporated
P880090 1990-07-03 MODEL 120UV ANTERIOR CHAMBER INTRAOCULAR LENS Bausch & Lomb Incorporated
P880082 1990-06-26 MODEL 14760 UV ABSORBING POSTERIOR CHAMBER LENSES Eyetech, LLC
P870045 1990-03-29 UV ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENES Bausch & Lomb Incorporated
P820044 1990-03-19 MODEL 91-50 IOL Bausch & Lomb Incorporated
P880010 1990-01-16 INTRAOCULAR LENS MODELS C118;C119;C138 AND C139 Alcon Laboratories, Inc.
P890068 1990-01-11 MODEL P-11 MODIFIED J-LOOP POSTERIOR CHAMBER IOL Chiron Ophthalmics
P850059 1989-12-11 KELMAN(TM) OMNIFIT II MODEL 2100 Bausch & Lomb Surgical, Inc.
P790027 1989-12-11 CHAMBER LENS MODELS G187G, G786B, G787B Bausch & Lomb Incorporated
P870075 1989-12-06 CLASSIC SERIES TM POSTERIOR CHAMBER INTRAOCULAR Newlensco
P870073 1989-11-30 STORZ POSTERIOR CHAMBER INTRAOCULAR LENSES Bausch & Lomb Incorporated
P820072 1989-11-20 CIRCULAR OPEN LOOP POSTERIOR IOLS & KRATZ ELLIPTIC Bausch & Lomb Incorporated
P830040 1989-10-10 8TYLES 30 & 31 POSTERIOR CHAMBER IOLS Alcon Research, LLC
P860059 1989-02-21 MODEL 304 (ULTRA C-LOOP) Advanced Medical Optics, Inc.
P820049 1988-04-27 MODELS PC10 & PC21 Advanced Medical Optics, Inc.
P870013 1988-03-31 IOLAB SUREFIT MODELS 85JS, 85JM & 85JL ANTERIOR Bausch & Lomb Incorporated
P810056 1987-12-07 MODEL AC10 & AC20 IOLS Advanced Medical Optics, Inc.
P820035 1987-11-03 OPTIFLEX ANTERIOR CHAMBER LENSES (L1-L5) Alcon, Inc.
P800017 1987-09-21 CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS Storz Ophthalmics, Inc.
P810018 1986-09-29 POSTERIOR CHAMBER INTRAOCULAR LENSES Alcon Laboratories, Inc.
P810001 1986-09-29 MODEL AC (AC1-AC5) Alcon, Inc.
P830033 1985-11-25 STYLE 17 & 17A POSTERIOR CHAMBER IOLS Advanced Vision Science, Inc.
P810042 1982-12-15 MODELS 011 & 011B IRIDOCAPSULAR IOLS Pharmacia, Inc.
P800027 1982-07-26 BINKHORST & FEDOROV I IRIS CLIP IOLS Storz Ophthalmics, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer