Data / Medical devices / Barrier, Absorbable, Adhesion
Barrier, Absorbable, Adhesion (MCN): 15 FDA-registered makers in 6 countries
15 establishments in 6 countries are registered with the FDA to make Barrier, Absorbable, Adhesion (product code MCN, Class 3). 8 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 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MCN
- Device class
- 3
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| United States | 10 |
| Belgium | 1 |
| Switzerland | 1 |
| France | 1 |
| United Kingdom | 1 |
| Ireland | 1 |
Makers of Barrier, Absorbable, Adhesion
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 |
|---|---|---|---|---|---|---|---|---|
| Baxter Healthcare Corporation | Round Lake, IL, United States | Complaint file establishment, Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Baxter R&D Europe SRL | Braine-l'Alleud Wallonia, Belgium | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon Sarl | Neuchatel, Switzerland | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon, Inc. | Somerville, NJ, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon, Inc. | Raritan, NJ, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon, LLC. | San Lorenzo, PR, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Rejoni, Inc | Bedford, MA, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Womed SAS | Montpellier Herault, France | Complaint file establishment, Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Anika Therapeutics, Inc. | Bedford, MA, United States | Contract manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | North Haven, CT, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fziomed, Inc. | San Luis Obispo, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Genzyme Corporation | Framingham, MA, United States | Contract manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Mast Biosurgery Usa Inc. | San Diego, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Terumo BCT, Ltd | LARNE Antrim and Newtownabbey, United Kingdom | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vantive Manufacturing Limited | CASTLEBAR, COUNTY MAYO Connaught, Ireland | 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.