Facility

Dynasthetics

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

Key facts

1recalls · worst Class II

3inspections · worst OAI

—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)	3008776780
Establishment type	Manufacture Medical Device
Location	3487 W 2100 S 300 Salt Lake City, UT, US 84119
Registration status	Active · expires 2026
Parent company	Dynasthetics (owner-operator 10034175)
Brand names	Sovant

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

Conserver, Oxygen
Product code NFB (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5905

Recalls & enforcement

Class IIOngoing2022-05-09
Due to a manufacturing issue that may result in filter leakage.

FDA inspections (3)

NAI2024-01-11
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2022-11-03
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2017-02-01
No Action Indicated · Compliance: Devices

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 Dynasthetics

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. “Dynasthetics (FEI 3008776780) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008776780-dynasthetics/

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