Serf
Country not established
- Devices
- 4
What Serf makes
Serf manufactures dual-mobility hip replacement systems, including acetabular cups and modular liners designed for primary and revision arthroplasty. Their portfolio includes metal-backed and ceramic-coated cup models, as well as modular components for use with their hip systems.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States and its products are listed in the FDA’s 510(k) registry.
Catalogue
BI-MENTUM dual mobility system Ref K181744
Regimes: 510(k) Registry: 510(k)Novae® Dual Mobility System, Hype® Hip System Ref K223745
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Serf have in the registry?
The registry currently lists 4 devices for Serf. Devices recorded under merged duplicate company entries are counted once.
Which registries list Serf's devices?
Among its 4 most recently registered devices, Serf has devices listed in FDA 510(k) (4 devices).
What risk classes do Serf's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Serf's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Serf in the registry?
The most recently registered devices listed for Serf include BI-MENTUM dual mobility system, Novae® Dual Mobility System, Hype® Hip System, NOVAE SUNFIT TH DUAL MOBILITY ACETABULAR CUP MODEL SUNFIT TH (METAL-BACK), NOVAE E TH DUAL MOBILITY ACETABULAR CUP MODEL and CI../..X liner for NOVAE Dual Mobility Acetabular Cup.