Facility

CHAMBERLAIN TECHNOLOGIES, LLC

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

Key facts

1recalls · worst Class II

1inspections · worst VAI

—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)	3015860534
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	21805 W Field Parkway Deer Park, IL, US 60010
Registration status	Active · expires 2026
Parent company	Chamberlain Technologies, LLC (owner-operator 10061294)
Brand names	SurgiMesh XD

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Mesh, Surgical, Polymeric
Product code FTL (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.3300

Recalls & enforcement

Class IICompleted2022-08-12
Potential presence of residual adhesive material on the mesh surface.

FDA inspections (1)

VAI2025-05-09
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

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.

All facilities operated by Chamberlain Technologies, LLC

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. “CHAMBERLAIN TECHNOLOGIES, LLC (FEI 3015860534) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3015860534-chamberlain-technologies-llc/

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