Facility

MEDICAL LASER TECHNOLOGIES LTD.

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)	3004529369
Establishment type	Manufacture Medical Device
Location	4 ZAPADNY PROEZD, BUILDING 4 ZELENOGRAD Moskva, RU 10346
Registration status	Active · expires 2026
Parent company	AEROLASE CORPORATION (owner-operator 9047647)
Brand names	LightPod Era; Era Elite

Activity by year

Recalls (1)

Devices registered here (1)

Powered Laser Surgical Instrument
Product code GEX (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4810

Recalls & enforcement

Class IITerminated2019-08-01
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device

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. “MEDICAL LASER TECHNOLOGIES LTD. (FEI 3004529369) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004529369-medical-laser-technologies-ltd/

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