Establishment Labs
Costa Rica CR-MF-000008155 Last updated 21 Oct 2026
- Devices
- 1,359
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Motiva Implants Ref SZC-650Q
Motiva Inflatable Balloon Ref MIB-0080
Motiva Flora Ref XMF-66
Motiva Implants Ref SZC-260
Motiva Implants Ref SZC-550Z
Motiva Implants Ref SZF-255
Motiva Implants Ref SZM-260Q
Motiva Implants Ref SZF-375Q
Motiva Implants Ref SZF-425Z
Motiva Implants Ref SZM-150
Motiva Implants Ref SZF-775Z
Motiva Implants Ref SZC-440Q
Motiva Implants Ref SZC-300Z
Motiva Implants Ref SZC-240
Motiva Implants Ref SZC-725
Motiva Implants Ref SZF-375
Motiva Implants Ref SZM-400
Motiva Flora Ref XML-54
Motiva Implants Ref SZD-245
Motiva Implants Ref SZC-410
Motiva Implants Ref SZM-290Z
Motiva Implants Ref SZF-145Z
Motiva Implants Ref SZM-105
Motiva Implants Ref SZF-355
Motiva Inflatable Balloon Ref MIB-0100
Motiva Implants Ref SZM-275
Motiva Flora Ref XML-66
Motiva Flora Ref XMF-70
Motiva Implants Ref SZF-220
Motiva Implants Ref SZC-925
Motiva Implants Ref SZC-825Q
Motiva Implants Ref SZC-300Q
Motiva Implants Ref SZD-625
Motiva Implants Ref SZD-475Z
Motiva Implants Ref SZD-190Z
Motiva Implants Ref SZC-210
Motiva Implants Ref SZF-450
Motiva Implants Ref SZD-625Z
Motiva Implants Ref SZM-475Z
Motiva Flora Ref XMF-54
Motiva Implants Ref SZD-230Q
Motiva Implants Ref SZD-320
Motiva Implants Ref SZD-230
Motiva Implants Ref SZC-590Q
Motiva Implants Ref SZD-300
Motiva Implants Ref SZM-310Z
Motiva Implants Ref SZF-550
Motiva Flora Ref XMM-70
Motiva Implants Ref SZD-180
Motiva Implants Ref SZD-575
Showing 1,301-1,350 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