Establishment Labs
Costa Rica CR-MF-000008155 Last updated 21 Oct 2026
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- Devices
- 599
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Motiva Implants Ref SZF-295Q
Motiva Implants Ref SZM-205Z
Motiva Implants Ref SZD-380
Motiva Implants Ref SZC-475Z
Motiva Implants Ref SZM-275Z
Motiva Implants Ref SZF-550Z
Motiva Implants Ref SZC-510
Motiva Implants Ref SZF-220Z
Motiva Implants Ref SZM-140
Motiva Injector Ref INJM-20
Motiva Implants Ref SZC-510Q
Motiva Flora Ref XMM-66
Motiva Implants Ref SZD-475Q
Motiva Implants Ref SZC-280
Motiva Implants Ref SZD-245Z
Motiva Inflatable Balloon Ref MIB-0090
Motiva Implants Ref SZM-150Z
Motiva Flora Ref XMM-58
Motiva Implants Ref SZD-155Q
Motiva Implants Ref SZM-220Q
Motiva Implants Ref SZC-590
Motiva Implants Ref SZD-360
Motiva Implants Ref SZC-1050
Motiva Implants Ref SZC-1050Z
Motiva Implants Ref SZD-265
Motiva Implants Ref SZD-215
Motiva Implants Ref SZC-380
Motiva Implants Ref SZC-350
Motiva Implants Ref SZD-285
Motiva Implants Ref SZD-205Q
Motiva Implants Ref SZM-170
Motiva Implants Ref SZC-650
Motiva Implants Ref SZF-400
Motiva Implants Ref SZF-275Q
Motiva Implants Ref SZC-350Q
Motiva Implants Ref SZM-525
Motiva Flora Ref XMM-54
Motiva Implants Ref SZD-180Q
Motiva Implants Ref SZM-105Z
Motiva Implants Ref SZM-220
Motiva Implants Ref SZF-775Q
Motiva Implants Ref SZM-400Q
Motiva Implants Ref SZD-380Q
Motiva Implants Ref SZC-210Z
Motiva Implants Ref SZC-380Z
Motiva Implants Ref SZD-265Q
Motiva Implants Ref SZC-300
Motiva Implants Ref SZF-450Q
Motiva Implants Ref SZD-205
Motiva Implants Ref SZM-430Q
Showing 551-600 of 599
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