Gelesis srl
Gelesis - Hydrogel-Based Medical Devices for Weight Management
Gelesis develops non-systemic superabsorbent hydrogels for weight management and GI-related chronic diseases, including Plenity.
- Type
- Manufacturer
- Location
- Calimera (LE), Italy
- Website
- https://www.gelesis.com
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- fda-registered (green), checked 2026-08-08 FDA
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- state-aid-sector (green), checked 2026-03-24 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registered-manufacturer (green), checked 2026-08-10 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
- vat-valid (green), checked 2026-08-08 VIES
- export-registered (green), checked 2026-08-08 EU EORI validation (European Commission)
Claimed certifications
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)