Facility

UIH 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)	3014809646
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	9380 Kirby Drive Houston, TX, US 77054
Registration status	Active · expires 2026
Parent company	UIH Technologies LLC (owner-operator 10059270)
Brand names	uMR Omega

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (2)

Coil, Magnetic Resonance, Specialty
Product code MOS (opens in a new tab) · Class II · Radiology · 21 CFR 892.1000
System, Nuclear Magnetic Resonance Imaging
Product code LNH (opens in a new tab) · Class II · Radiology · 21 CFR 892.1000

Recalls & enforcement

Class IIOngoing2025-09-12
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

FDA inspections (1)

VAI2025-08-20
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 UIH 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. “UIH TECHNOLOGIES, LLC (FEI 3014809646) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3014809646-uih-technologies-llc/

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