Facility

LISA LASER PRODUCTS GMBH

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)	3003168101
Establishment type	Manufacture Medical Device
Location	ALBERT-EINSTEIN-STR. 4 KATLENBURG-LINDAU Lower Saxony, DE 37191
Registration status	Active · expires 2026
Parent company	OMNIGUIDE, INC. (owner-operator 9070939)
Brand names	Powered laser surgical instrument - Sphinx Jr.

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 IITerminated2012-11-05
Failure of glue joint, allowed a portion of the single use device to shift inside, may separate and fall into the patient

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. “LISA LASER PRODUCTS GMBH (FEI 3003168101) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003168101-lisa-laser-products-gmbh/

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