Data / Medical devices / Netherlands / ABBVIE Logistics BV, Inc
ABBVIE Logistics BV, Inc: FDA-registered device maker in Zwolle Overijssel, Netherlands, 1 510(k) clearance
ABBVIE Logistics BV, Inc is registered with the FDA (registration 3013307971) in Zwolle Overijssel, Netherlands. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 17, 2013. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3013307971
- Address
- Zuiderzeelaan 53, Zwolle Overijssel, Netherlands, 8017 JV
- Owner or operator
- AbbVie, Inc. (2011068)
- Roles
- Exporter to the US
- First device listed
- January 23, 2015
- Registered through
- 2027
- Brand names listed
- Fill Tube Kit, Insertion Sleeve; Keller Funnel; Keller Funnel 2, Strattice Reconstructive Tissue Matrix (RTM) Laparoscopic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Kit, Surgical Instrument, Disposable | KDD | 1 | Exporter to the US | accessdata.fda.gov |
| Mesh, Surgical | FTM | 2 | Exporter to the US | accessdata.fda.gov |
| Mesh, Surgical, Collagen, Large Abdominal Wall Defects | OXK | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 17, 2013 | K130817 | LTN - LAPAROSCOPIC SURGICAL MESH | OXK | Substantially Equivalent | Lifecell Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Mesh, Surgical
- All makers of Mesh, Surgical, Collagen, Large Abdominal Wall Defects
- All makers of Kit, Surgical Instrument, Disposable
Updated April 17, 2013. 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.