ABB Optical Group LLC.

FDA Device Registration & Listing · Kansas City, MO, US · Registration 2916547

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2916547
FEI Number
2916547
Entity Name
ABB Optical Group LLC.
City/State/Country
Kansas City, MO, US
Establishment Address
3901 Ne 33rd Ter Ste E, Kansas City, MO 64117, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ABB OPTICAL GROUP, LLC (Owner Number: 10036093)
Owner / Operator Contact Address
3901E NE 33rd Terrace, Kansas City, MO 64117, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CONCISE CONCISE CONCISE CONCISE Concise Custom Soft Contact Lens CONCISE CONCISE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2011-04-19

Official Correspondent

John Kenyon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ABB OPTICAL GROUP, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K133079 Alden Optical Labs., Inc. IO2 SPHER(MANGOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IO2 TORIC (MANGOFILCON A) SOFT (HYDROPHILIC) 2013-12-17
K941998 Ocu-Ease Optical Products, Inc. OCU-FLEX-38 (POLYMACON) 1994-10-13
K992500 Cantor & Silver , Ltd. CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS 1999-08-18
K984098 Adventures IN Color Technology, Ltd. ADVENTURE TINTS, COLOR ENHANCED TINTED SOFT CONTACT LENS 1999-05-10
K003161 Les Laboratoires Blanchard ESSTECH MULTI TORIC ASPHERIC (MULTIFOCAL) (HIOXIFILCON B) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR (CLEAR AND TINT 2000-12-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0018-07 Ciba Vision Corporation 2
CSI Daily Wear, soft (hydrophilic) contact lenses
Z-0019-07 Ciba Vision Corporation 2
CSI Flexible Wear, soft (hydrophilic) contact lenses
Z-0020-07 Ciba Vision Corporation 2
CSI Toric, soft (hydrophilic) contact lenses
Z-0044-2012 CooperVision Inc. 2
AVAIRA Toric (enfilcon A) TORIC soft (Hydrophilic) Contact Lenses, 6 SOFT CONTACT LENSES FOR ASTIGMATISM, CooperVision, Scottsville, NY 14546 USA; Juana Diaz, PR 00795 USA; Hamble SO31, 4RF, UK; Device Listing # D033736. Product Usage: Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) in aphakic and non-aphakic persons with non-diseased eyes in powers from -20.00- to +20.00 diopters and astigmatic corrections from -0.25 to -10.00 diopters. The AVAIRA Soft Contact Lens is indicated for single - use disposable wear and daily wear. When prescribed for frequent replacement, the lens may be disinfected using a chemical or hydrogen peroxide disinfecting system.
Z-0326-2026 Alcon Research LLC 2
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2916547. Last updated year: 2026. Please use registration number 2916547 when referencing this establishment in official correspondence.
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