Establishment Labs
Costa Rica CR-MF-000008155 Last updated 21 Oct 2026
- Devices
- 1,359
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Motiva Implants Ref E2OF-460Z
Motiva Implants Ref E2OM-240T
Motiva Implants Ref E2OF-620Z
Motiva Implants Ref ERSC-510
Motiva Implants Ref DSF-190
Motiva Implants Ref RVD-300+
Motiva Implants Ref RVF-295+Z
Motiva Implants Ref ERVC-325Z
Motiva Implants Ref RSF-235+
Motiva Implants Ref ERVD-380
Motiva Implants Ref ERSM-290Z
Motiva Implants Ref E2SF-215
Motiva Implants Ref ERSM-150Z
Motiva Implants Ref E2SF-355
Motiva Implants Ref E2SM-180Z
Motiva Implants Ref E2SM-130T
Motiva Implants Ref E2SD-285
Motiva Implants Ref E2OF-510
Motiva Implants Ref DSD-220Z
Motiva Implants Ref RVD-190+
Motiva Implants Ref E2SF-595
Motiva Implants Ref ERSC-180
Motiva Implants Ref DSD-120
Motiva Implants Ref ERVD-245Z
Motiva Implants Ref E2SC-290
Motiva Implants Ref DSC-270Z
Motiva Implants Ref E2OM-275
Motiva Implants Ref ERVD-475
Motiva Implants Ref E2SF-135
Motiva Implants Ref E2SF-275T
Motiva Implants Ref ERVM-205
Motiva Implants Ref E2SC-860
Motiva Implants Ref ERSC-410Z
Motiva Implants Ref ERSC-825Z
Motiva Implants Ref RVF-400+Z
Motiva Implants Ref DSC-485T
Motiva Implants Ref E2OC-410
Motiva Implants Ref RVF-775+
Motiva Implants Ref E2SD-170
Motiva Implants Ref E2SF-400Z
Motiva Implants Ref E2SD-500T
Motiva Implants Ref E2SF-595Z
Motiva Implants Ref RSM-170+Z
Motiva Implants Ref E2OD-635T
Motiva Implants Ref ERSC-440Z
Motiva Implants Ref ERVD-320Z
Motiva Implants Ref RVM-400+
Motiva Implants Ref ERVD-190Z
Motiva Implants Ref E2SM-200
Motiva Implants Ref ERSF-275Z
Showing 151-200 of 1,359
EUDAMED certificates
Notified body 2797 4 certificates
- MDR 798371 Supplemented
Technical documentation EU MDR
- Issued
- 12 Jun 2026
- Expires
- 1 Jan 2030
- Reason
- Change approved
- MDR 768275 Supplemented
Technical documentation EU MDR
- Issued
- 12 Jun 2026
- Expires
- 5 Jan 2028
- Reason
- Change approved
- MDR 768277 Supplemented
Technical documentation EU MDR
- Issued
- 12 Jun 2026
- Expires
- 5 Jan 2028
- Reason
- Change approved
- MDR 745219 Supplemented
Technical documentation EU MDR
- Issued
- 12 Jun 2026
- Expires
- 22 May 2027
- Reason
- Change approved
Related companies
Authorised representatives
Notified bodies
- Notified body 2797
About
A global medical technology company dedicated to improving women’s health and wellness through the power of science, engineering, and technology.
What Establishment Labs makes
Establishment Labs manufactures a range of vaginal health devices, including injectable solutions, inflatable balloons, and various implantable products under the Motiva brand. These products are designed for medical applications in pelvic floor and vaginal tissue treatment, such as tissue augmentation and structural support.
The company’s devices are classified under EU regulations as Class I, Class IIa, and Class III, with listings maintained in the EUDAMED database. The manufacturer is based in Costa Rica and adheres to relevant regulatory frameworks for medical devices in the European market.
Frequently asked questions
What types of medical devices does Establishment Labs manufacture?
Establishment Labs specializes in vaginal health devices under the Motiva brand. These include injectable solutions like the Motiva Injector, inflatable balloons for temporary tissue expansion, and multiple types of Motiva Implants designed for long-term structural support or augmentation. The devices are primarily focused on pelvic floor and vaginal tissue treatments.
Where is Establishment Labs based, and how does that affect its regulatory compliance?
Establishment Labs is based in Costa Rica, which means it operates under the regulatory frameworks of that country while also complying with EU requirements for devices sold in the European market. Since its products are listed in the EUDAMED database, they must meet EU Medical Device Regulations (MDR) or Medical Device Directives (MDD) standards, including classification under Class I, IIa, or III.
Which regulatory registries list Establishment Labs’ devices, and why is this important?
Establishment Labs’ devices are listed in the EUDAMED database, which is the official EU registry for medical devices. This listing is critical because it provides transparency on device authorizations, classifications, and regulatory status within the European Economic Area. It helps healthcare professionals, regulators, and authorities verify compliance with EU requirements.
How are Establishment Labs’ devices classified under EU regulations, and what does that mean?
Establishment Labs’ devices are classified as Class I, Class IIa, or Class III under EU Medical Device Regulations. Classification determines the level of scrutiny and regulatory requirements for each product. For example, Class III devices—such as some implants—require rigorous clinical evidence and strict manufacturing controls due to higher risk, while Class I devices (like certain injectors) may have fewer regulatory hurdles but still must meet safety and performance standards.
Information
- Country
- Costa Rica
- Address
- Coyol Free Zone & Business Park Building 4th street, building B15 Alajuela Costa Rica, Alajuela, Costa Rica
- Website
- establishmentlabs.com
- [email protected]
- Phone
- +506 2434-2400
- PRRC contact
- Alberto Quesada Rivera
- EUDAMED SRN
- CR-MF-000008155