Data / Medical devices / Germany / PHARMAMONDIS GmbH

PHARMAMONDIS GmbH: FDA-registered device maker in Munich Bavaria, Germany, 13 PMA approvals

Name: PHARMAMONDIS GmbH FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

PHARMAMONDIS GmbH is registered with the FDA (registration 3026391021) in Munich Bavaria, Germany. It lists 3 device types. The FDA files 13 PMA approvals under its listings, the newest dated October 19, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3026391021
Address: Levelingstr. 8, Munich Bavaria, Germany, 81673
Owner or operator: Pharmamondis (10087335)
Roles: Exporter to the US, Repackager or relabeler
First device listed: February 14, 2023
Registered through: 2026

Devices it lists

Device	Product code	Class	Role	Source
Acid, Hyaluronic, Intraarticular	MOZ	3	Exporter to the US, Repackager or relabeler	accessdata.fda.gov
Implant, Dermal, For Aesthetic Use	LMH	3	Exporter to the US, Repackager or relabeler	accessdata.fda.gov
Implant, Dermal, For Aesthetic Use In The Hands	PKY	3	Exporter to the US, Repackager or relabeler	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
October 19, 2017	P170002	RHA 2, RHA 3, RHA 4	LMH	55	August 31, 2026	accessdata.fda.gov
August 29, 2017	P170007	DUROLANE	MOZ	15	December 23, 2025	accessdata.fda.gov
December 9, 2016	P140029	Restylane Refyne, Restylane Defyne	LMH	51	September 18, 2026	accessdata.fda.gov
February 25, 2014	P090031	MONOVISC	MOZ	15	August 8, 2023	accessdata.fda.gov
October 22, 2013	P110033	JUVEDERM VOLUMA XC	LMH	97	August 28, 2026	accessdata.fda.gov
November 14, 2011	P090016	BELOTERO BALANCE	LMH	60	May 3, 2026	accessdata.fda.gov
December 22, 2006	P050052	RADIESSE INJECTABLE IMPLANT	LMH	169	June 26, 2026	accessdata.fda.gov
June 2, 2006	P050047	JUVEDERM 24HV, JUVEDERM 30 AND JUVEDERM 30HV GEL IMPLANTS	LMH	101	August 28, 2026	accessdata.fda.gov
March 25, 2005	P040024	RESTYLANE INJECTABLE GEL	LMH	132	March 12, 2026	accessdata.fda.gov
August 3, 2004	P030050	SCULPTRA AND SCULPTRA AESTHETIC	LMH	54	September 17, 2026	accessdata.fda.gov
February 4, 2004	P030019	ORTHOVISC HIGH MOLECULAR WEIGHT HYALURONAN	MOZ	23	August 28, 2026	accessdata.fda.gov
January 24, 2001	P980044	SUPARTZ FX	MOZ	62	September 4, 2026	accessdata.fda.gov
August 8, 1997	P940015	SYNVISC ONE	MOZ	51	January 2, 2025	accessdata.fda.gov

Compare with other makers

Updated August 31, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.