Data / Medical devices / Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations
Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations (KGG): 4 FDA-registered makers in 2 countries
4 establishments in 2 countries are registered with the FDA to make Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations (product code KGG, Class 3). 3 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 1 recall event (1 Class I). FDA data exported November 2, 2026.
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- Product code
- KGG
- Device class
- 3
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| United States | 3 |
| Switzerland | 1 |
Makers of Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cerenovus, Inc. | Miami, FL, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Cerenovus, Inc. | Raynham, MA, United States | Manufacturer | 0 | 1 | 1 | 1 | api.fda.gov | |
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Chemence Medical Inc. | Alpharetta, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.