Facility

NEW MEDICAL TECHNOLOGIES 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)	3008252257
Establishment type	Manufacture Medical Device
Location	Freiburgstrasse 453 Bern, CH 3018
Registration status	Active · expires 2026
Parent company	New Medical Technologies GmbH (owner-operator 10031563)
Brand names	Cryosolutions

Activity by year

Recalls (1)

Devices registered here (1)

Unit, Cryosurgical, Accessories
Product code GEH (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4350

Recalls & enforcement

Class IIOngoing2024-12-19
During the assembly of the cartridge to its connecting body part, the valve may open prematurely resulting in partial or complete emptying of the cartridge before its intended use.

All facilities operated by New Medical Technologies GmbH

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. “NEW MEDICAL TECHNOLOGIES GMBH (FEI 3008252257) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008252257-new-medical-technologies-gmbh/

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