Facility

EKLA CORPORATION

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)	3008733163
Establishment type	Repack or Relabel Medical Device
Location	1707 Quincy Ave Ste 127 Naperville, IL, US 60540
Registration status	Active · expires 2026
Parent company	EKLA Corporation (owner-operator 10035863)
Brand names	EKLA FINGER PULSE OXIMETER, E02-1001; NOVAPLUS FINGER PULSE OXIMETER, V02-1001

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 IITerminated2016-10-20
Incorrect hCG results

All facilities operated by EKLA Corporation

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. “EKLA CORPORATION (FEI 3008733163) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008733163-ekla-corporation/

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