Facility

MED-HOT THERMAL IMAGING, INC

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)	3006033213
Establishment type	Manufacture Medical Device
Location	2502 Ewell Road Lakeland, FL, US 33811
Registration status	Active · expires 2026
Parent company	MED-HOT THERMAL IMAGING, INC (owner-operator 9094861)
Brand names	Max 76 and Max 307

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

System, Telethermographic (Adjunctive Use)
Product code LHQ (opens in a new tab) · Class I · Obstetrics/Gynecology · 21 CFR 884.2980

Recalls & enforcement

Class IITerminated2017-01-14
Indications for use are not cleared or approved for market in the U.S.

FDA inspections (1)

VAI2017-01-11
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 MED-HOT THERMAL IMAGING, 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. “MED-HOT THERMAL IMAGING, INC (FEI 3006033213) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006033213-med-hot-thermal-imaging-inc/

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