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UPS Supply Chain Solutions, Inc.: FDA-registered device maker in Ostrava-Poruba Ostrava-Mesto, Czechia, 4 510(k) clearances and 1 PMA approval

Name: UPS Supply Chain Solutions, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

UPS Supply Chain Solutions, Inc. is registered with the FDA (registration 3044853379) in Ostrava-Poruba Ostrava-Mesto, Czechia. It lists 3 device types. The FDA files 4 510(k) clearances and 1 PMA approval under its listings, the newest dated April 25, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3044853379
Address: 17 Listopadu 6242, Ostrava-Poruba Ostrava-Mesto, Czechia, 708 00
Owner or operator: UPS Supply Chain Solutions, Inc. (10038314)
Roles: Repackager or relabeler
First device listed: March 16, 2026
Registered through: 2026
Brand names listed: DAILES AquaComfort Plus Toric, DAILIES TOTAL 1 for Astigmatism, Precision1 for Astigmatism, Precision7 for Astigmatism, Total30 Multifocal, Total30 for Astigmatism

Devices it lists

Device	Product code	Class	Role	Source
Lens, Contact, (Disposable)	MVN	2	Repackager or relabeler	accessdata.fda.gov
Lenses, Soft Contact, Daily Wear	LPL	2	Repackager or relabeler	accessdata.fda.gov
Lenses, Soft Contact, Extended Wear	LPM	3	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
April 12, 2021	K210436	Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere	LPL	Substantially Equivalent	Alcon Laboratories, Inc.	accessdata.fda.gov
January 18, 2019	K182782	DAILIES TOTAL1, DAILIES TOTAL1 Asphere, DAILIES TOTAL1 for ASTIGMATISM, DAILIES TOTAL1 Multifocal, DAILIES TOTAL1 Multifocal Toric	LPL	Substantially Equivalent	Alcon Laboratories, Inc.	accessdata.fda.gov
December 11, 2018	K182902	Precision1	LPL	Substantially Equivalent	Alcon Laboratories, Inc.	accessdata.fda.gov
February 21, 2013	K123994	DAILIES AQUACOMFORT PLUS, DAILIES AQUACOMFORT PLUS TORIC, DAILIES AQUACOMFORT PLUS MULTIFOCAL	LPL	Substantially Equivalent	Ciba Vision Corporation	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
April 25, 2023	P220007	Precision7; Precision7 for Astigmatism; Precision7 Multifocal; Precision7 Multifocal Toric (serafilcon A) Soft Conta	LPM	7	March 11, 2026	accessdata.fda.gov

Compare with other makers

Updated March 11, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.