UPS Supply Chain Solutions, Inc.

FDA Device Registration & Listing · Ostrava-Poruba Ostrava-Mesto, CZ · Registration 3044853379

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
3044853379
FEI Number
3044853379
Entity Name
UPS Supply Chain Solutions, Inc.
City/State/Country
Ostrava-Poruba Ostrava-Mesto, CZ
Establishment Address
17 Listopadu 6242, Ostrava-Poruba Ostrava-Mesto 708 00, CZ
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
UPS Supply Chain Solutions, Inc. (Owner Number: 10038314)
Owner / Operator Contact Address
12380 Morris Road, Alpharetta, GA 30005, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Total30 Multifocal Total30 for Astigmatism Precision7 for Astigmatism DAILES AquaComfort Plus Toric DAILIES TOTAL 1 for Astigmatism Precision1 for Astigmatism

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MVN Lens, Contact, (Disposable) Ophthalmic Class 2 886.5925 2026-03-16
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2026-03-16
LPM Lenses, Soft Contact, Extended Wear Ophthalmic Class 3 886.5925 2026-03-16
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2026-03-16
MVN Lens, Contact, (Disposable) Ophthalmic Class 2 886.5925 2026-03-16
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2026-03-16
MVN Lens, Contact, (Disposable) Ophthalmic Class 2 886.5925 2026-03-16
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2026-03-16
MVN Lens, Contact, (Disposable) Ophthalmic Class 2 886.5925 2026-03-16

Official Correspondent

Sam Waltham

US Agent Details

Sam Waltham Business: UPS SUPPLY CHAIN SOLUTIONS, INC. Email: ralicensing@ups.com Phone: (678) 7463231

Related Public Records

Same Entity

UPS Supply Chain Solutions, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3009637528 UPS Supply Chain Solutions, Inc. Mira Loma, CA, US

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-0326-2026 Alcon Research LLC 2
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044853379. Last updated year: 2026. Please use registration number 3044853379 when referencing this establishment in official correspondence.
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