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 SZD-155Z
Motiva Implants Ref SZF-255Q
Motiva Implants Ref SZF-700Q
Motiva Implants Ref SZC-260Q
Motiva Implants Ref SZF-220Q
Motiva Implants Ref SZD-135Z
Motiva Flora Ref MFPL-001
Motiva Flora Ref XMF-74
Motiva Implants Ref SZC-410Q
Motiva Implants Ref SZF-425
Motiva Implants Ref SZF-145Q
Motiva Implants Ref SZD-285Q
Motiva Implants Ref SZF-175Q
Motiva Flora Ref XML-62
Motiva Implants Ref SZD-340
Motiva Implants Ref SZM-230Q
Motiva Implants Ref SZM-205
Motiva Implants Ref SZM-125Q
Motiva Implants Ref SZM-140Z
Motiva Implants Ref SZD-425
Motiva Flora Ref XMM-62
Motiva Implants Ref SZC-825
Motiva Flora Ref XML-58
Motiva Implants Ref SZC-325
Motiva Flora Ref XMF-58
Motiva Implants Ref SZM-125Z
Motiva Implants Ref SZC-180Z
Motiva Implants Ref SZC-180
Motiva Implants Ref SZF-295
Motiva Implants Ref SZC-280Z
Motiva Implants Ref SZD-320Q
Motiva Implants Ref SZF-145
Motiva Implants Ref SZC-440
Motiva Implants Ref SZF-275Z
Motiva Implants Ref SZF-335
Motiva Implants Ref SZC-475
Motiva Implants Ref SZD-525
Motiva Implants Ref SZC-240Z
Motiva Implants Ref SZF-205
Motiva Implants Ref SZD-340Z
Motiva Injector Ref INJM-23
Motiva Implants Ref SZF-700
Motiva Implants Ref SZD-135
Motiva Implants Ref SZD-360Q
Motiva Implants Ref SZF-275
Motiva Implants Ref SZM-160
Motiva Implants Ref SZM-170Q
Motiva Implants Ref SZF-775
Motiva Implants Ref SZD-575Z
Motiva Implants Ref SZM-360Z
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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