Data / Medical devices / Spain / Anatomical Geometry S.L.
Anatomical Geometry S.L.: FDA-registered device maker in MAIRENA DEL ALJARAFE Sevilla, Spain, 1 510(k) clearance
Anatomical Geometry S.L. is registered with the FDA (registration 3044735888) in MAIRENA DEL ALJARAFE Sevilla, Spain. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 22, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044735888
- Address
- C/ Formacion, 6, MAIRENA DEL ALJARAFE Sevilla, Spain, 41927
- Owner or operator
- Anatomical Geometry S.L. (10095345)
- Roles
- Foreign private label distributor, Manufacturer
- First device listed
- March 2, 2026
- Registered through
- 2026
- Brand names listed
- eXaCast Thermoplastic Mask, eXaSkin Plus, eaSyFix
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Block, Beam-Shaping, Radiation Therapy | IXI | 2 | Manufacturer | accessdata.fda.gov |
| Cradle, Patient, Radiologic | KXH | 1 | Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| System, Planning, Radiation Therapy Treatment | MUJ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 22, 2026 | K252784 | eXaSkin Plus | MUJ | Substantially Equivalent | Anatomical Geometry S.L. | accessdata.fda.gov |
Compare with other makers
- All makers of Block, Beam-Shaping, Radiation Therapy
- All makers of System, Planning, Radiation Therapy Treatment
- All makers of Cradle, Patient, Radiologic
Updated May 22, 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.