Data / Medical devices / Germany / MERZ AESTHETICS Dessau
MERZ AESTHETICS Dessau: FDA-registered device maker in Dessau Saxony-Anhalt, Germany, 1 PMA approval
MERZ AESTHETICS Dessau is registered with the FDA (registration 3036164410) in Dessau Saxony-Anhalt, Germany. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated May 19, 2026. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3036164410
- Address
- Am Pharmapark, Dessau Saxony-Anhalt, Germany, 06861
- Owner or operator
- Merz Aesthetics (10095918)
- Roles
- Manufacturer
- First device listed
- May 21, 2026
- Registered through
- 2027
- Brand names listed
- Belotero Volume (+) Lidocaine
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Implant, Dermal, For Aesthetic Use | LMH | 3 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| May 19, 2026 | P250020 | Belotero Volume (+) Lidocaine | LMH | 4 | September 10, 2026 | accessdata.fda.gov |
Compare with other makers
Updated September 10, 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.