Facility

SENSORY MEDICAL INC

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

Key facts

1recalls · worst Class I

—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)	3016541541
Establishment type	Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198
Location	1580 Logan Street Denver, CO, US 80203
Registration status	Active · expires 2026
Parent company	Sensory Medical Inc (owner-operator 10062257)
Brand names	TECHNOLOGY HUB

Activity by year

Recalls (1)

Devices registered here (1)

Monitor, Bed Patient
Product code KMI (opens in a new tab) · Class I · General Hospital · 21 CFR 880.2400

Recalls & enforcement

Class IOngoing2022-03-14
Due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.

All facilities operated by Sensory Medical Inc

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. “SENSORY MEDICAL INC (FEI 3016541541) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3016541541-sensory-medical-inc/

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