Is this your brand? Sign in to claim ownership.
Sign in to claim this brandEstablishment Labs S.A.
US
Last updated May 23, 2026
What Establishment Labs S.A. makes
Establishment Labs S.A. manufactures silicone gel-filled breast implants with smooth surfaces, designed for reconstructive and cosmetic procedures. Their portfolio also includes skin-port tissue expanders, which are used in staged breast reconstruction to gradually expand tissue before implant placement.
The company’s devices are classified as Class III under FDA regulations, indicating they require premarket approval due to their substantial risk. These products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device reporting requirements.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Establishment Labs S.A. manufacture?
Establishment Labs S.A. specializes in silicone gel-filled breast implants with smooth surfaces, primarily used for reconstructive and cosmetic procedures. They also produce skin-port tissue expanders, which are essential in staged breast reconstruction to gradually expand tissue before implant placement.
Where is Establishment Labs S.A. based?
The company is based in the United States, as indicated by its regulatory and manufacturing context.
Which regulatory registries list Establishment Labs S.A.’s devices?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, which ensures traceability and compliance with U.S. medical device reporting requirements. This registry helps track and monitor devices for regulatory purposes.
How are Establishment Labs S.A.’s devices classified under U.S. regulations?
The devices manufactured by Establishment Labs S.A. fall under Class III classification by the FDA. This classification is assigned to high-risk medical devices that require premarket approval due to their potential risks and benefits, ensuring rigorous evaluation before market authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 853166098
Catalogue (176)
Page 1 of 4Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Establishment Labs S.a. Coyol Alajuela · CR FEI 3012883202