Facility

IANTREK INC.

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)	3017891009
Establishment type	Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198
Location	295 Promenade Street, Suite 101 Providence, RI, US 02908
Registration status	Active · expires 2026
Parent company	Iantrek Inc. (owner-operator 10079930)
Brand names	CycloPen; AlloSert Canal; AlloSert UVEO; Spannula

Activity by year

Recalls (1)

Devices registered here (1)

Cannula, Ophthalmic
Product code HMX (opens in a new tab) · Class I · Ophthalmic · 21 CFR 886.4350

Recalls & enforcement

Class IIOngoing2025-09-06
Potential for compromised integrity of the sterile packaging.

All facilities operated by Iantrek Inc.

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. “IANTREK INC. (FEI 3017891009) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3017891009-iantrek-inc/

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