Van Dellen, Ltd.
Country not established
- Devices
- 7
What Van Dellen, Ltd. makes
Van Dellen, Ltd. manufactures sterile surgical instruments and accessories for ophthalmic and procedural use, including bacteria filters, retrobulbar needles, aspirators, irrigating cystotomes, cannulas, and specialized tubing for fluid management. Their portfolio also includes a Healon cannula designed for viscoelastic substance delivery in eye surgeries.
The company’s devices are classified under FDA’s Class I and Class II regulations, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Van Dellen Bacteria Filter Ref K873465
Regimes: 510(k) Registry: 510(k)Van Dellen Retrobulbar Needle Ref K873162
Regimes: 510(k) Registry: 510(k)Van Dellen Aspirator Ref K873462
Regimes: 510(k) Registry: 510(k)Van Dellen Irrigating Cystotome Ref K873163
Regimes: 510(k) Registry: 510(k)Van Dellen Cannula Ref K873464
Regimes: 510(k) Registry: 510(k)Van Dellen Healon Cannula Ref K873164
Regimes: 510(k) Registry: 510(k)Van Dellen Aspirating Tubing Ref K873463
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Van Dellen, Ltd. have in the registry?
The registry currently lists 7 devices for Van Dellen, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Van Dellen, Ltd.'s devices?
Among its 7 most recently registered devices, Van Dellen, Ltd. has devices listed in FDA 510(k) (7 devices).
What risk classes do Van Dellen, Ltd.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Van Dellen, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Van Dellen, Ltd. in the registry?
The most recently registered devices listed for Van Dellen, Ltd. include VAN DELLEN BACTERIA FILTER, VAN DELLEN RETROBULBAR NEEDLE, VAN DELLEN ASPIRATOR and VAN DELLEN IRRIGATING CYSTOTOME.