Serral, S.A. DE C.V.
Country not established
- Devices
- 6
What Serral, S.A. DE C.V. makes
Serral, S.A. de C.V. manufactures surgical sutures and ligatures, including absorbable and non-absorbable variants, designed for use in general and specialty surgical procedures. Their portfolio includes braided and monofilament sutures, as well as specialized products like coated and monofilament absorbable sutures for specific tissue applications.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device authorisation requirements. The manufacturer operates from the United States.
Catalogue
Serralester Ref K020902
Regimes: 510(k) Registry: 510(k)Serralapg Ref K033762
Regimes: 510(k) Registry: 510(k)Serralsilk Ref K020901
Regimes: 510(k) Registry: 510(k)Serralene, Model Catalog No 1S Ref K020265
Regimes: 510(k) Registry: 510(k)Serralgut Ref K020597
Regimes: 510(k) Registry: 510(k)Serralnyl Ref K020146
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Serral, S.A. DE C.V. have in the registry?
The registry currently lists 6 devices for Serral, S.A. DE C.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Serral, S.A. DE C.V.'s devices?
Among its 6 most recently registered devices, Serral, S.A. DE C.V. has devices listed in FDA 510(k) (6 devices).
What risk classes do Serral, S.A. DE C.V.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Serral, S.A. DE C.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Serral, S.A. DE C.V. in the registry?
The most recently registered devices listed for Serral, S.A. DE C.V. include SERRALESTER, SERRALAPG, SERRALSILK and SERRALENE, MODEL CATALOG NO 1S.