Facility

Alcon Research, LLC

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

2inspections · worst NAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1610287
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	6201 SOUTH FREEWAY Fort Worth, TX, US 76134
Registration status	Active · expires 2026
Parent company	Alcon Laboratories, Inc. (owner-operator 1610287)

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (2)

Lens, Contact, (Disposable)
Product code MVN (opens in a new tab) · Class II · Ophthalmic · 21 CFR 886.5925
Lenses, Soft Contact, Daily Wear
Product code LPL (opens in a new tab) · Class II · Ophthalmic · 21 CFR 886.5925

Recalls & enforcement

Class IITerminated2018-07-17
Potential for the optical head to detach from the stand due to the lack of thread adhesive.

FDA inspections (2)

NAI2019-10-24
No Action Indicated · Bioresearch Monitoring
NAI2016-01-28
No Action Indicated · Project Evaluation: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Alcon Research, LLC (FEI 1610287) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1610287-alcon-research-llc/

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