Facility

CIBA VISION ASIAN MANUFACTURING AND LOGISTICS Pte. Ltd.

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

Key facts

1recalls · worst Class II

—inspections in our data

—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)	3003657720
Establishment type	Manufacture Medical Device
Location	133 TUAS SOUTH AVENUE 3 SINGAPORE South West, SG 63755
Registration status	Active · expires 2026
Parent company	Alcon Laboratories, Inc. (owner-operator 1610287)

Activity by year

Recalls (1)

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.

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. “CIBA VISION ASIAN MANUFACTURING AND LOGISTICS Pte. Ltd. (FEI 3003657720) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003657720-ciba-vision-asian-manufacturing-and-logi/

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