Coletica S.A.
Country not established
- Devices
- 1
What Coletica S.A. makes
Coletica S.A. manufactures absorbable collagen-based hemostatic sponges designed to control bleeding during surgical procedures. These products are intended for use in minimally invasive and open surgeries where rapid clotting is required, such as in vascular, cardiac, or trauma applications.
The company’s portfolio is regulated under Class III devices in the U.S., requiring Premarket Approval (PMA) authorization through the FDA. The products are listed under the FDA’s PMA registry, and the manufacturer is based in the United States.
Catalogue
Actifoam Absorbable Collagen Hemostatic Sponge Ref P930030
Regimes: PMA, withdrawn Registry: PMA
Frequently asked questions
How many devices does Coletica S.A. have in the registry?
The registry currently lists 1 device for Coletica S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coletica S.A.'s devices?
Among its 1 most recently registered device, Coletica S.A. has devices listed in FDA PMA (1 device).
What risk classes do Coletica S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Coletica S.A.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Coletica S.A. in the registry?
The most recently registered devices listed for Coletica S.A. include ACTIFOAM ABSORBABLE COLLAGEN HEMOSTATIC SPONGE.