RegWardenFDA facility compliance records
Facility

OMM IMPORTS, INC. D/B/A ZERO GRAVITY

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

Activity by year

FDA actions on record by year2022: 1 recalls, 1 inspections20172018201920202021220222023202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

  • Lamp, Infrared, Therapeutic Heating
    Product code ILY (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5500

Recalls & enforcement

  • Class IIOngoing2022-09-01
    The firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed to provide safety information, reproductions and locations of the labels, and a warning statement in the user manual.

FDA inspections (1)

  • NAI2022-09-09
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices; Radiation Control and Health Safety Act · 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.

Related

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. “OMM IMPORTS, INC. D/B/A ZERO GRAVITY (FEI 3012327767) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3012327767-omm-imports-inc-d-b-a-zero-gravity/

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