Facility

NOX MEDICAL

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)	3007389703
Establishment type	Repack or Relabel Medical Device
Location	Katrinartuni 2 Reykjavik, IS IS-105
Registration status	Active · expires 2026
Parent company	Nox Medical (owner-operator 10027652)

Activity by year

Recalls (1)

Devices registered here (1)

Oximeter
Product code DQA (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2700

Recalls & enforcement

Class IITerminated2021-09-07
Error in the device firmware results in the inaccurate detection of device position.

All facilities operated by Nox Medical

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. “NOX MEDICAL (FEI 3007389703) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007389703-nox-medical/

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