Landanger
Country not established FDA
- Devices
- 3,284
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Landanger makes
The company manufactures reusable surgical instruments, including general-purpose scissors, soft-tissue manipulation forceps (both tweezers-like and scissors-like designs), suturing needle holders, retraction systems, retractor blades, and self-retaining retractors. Their portfolio also includes reusable instrument trays designed for surgical procedures.
All devices fall under Class I regulatory classification and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Catalogue
Search and filter all 3,284 devicesShowing 1-50 of 3,284
Company details
- DUNS number
- 299889175
FDA establishments
- Landanger CHAUMONT Haute-Marne · FR FEI 3005182241
Frequently asked questions
How many devices does LANDANGER have in the registry?
The registry currently lists 3284 devices for LANDANGER. Devices recorded under merged duplicate company entries are counted once.
Which registries list LANDANGER's devices?
Among its 50 most recently registered devices, LANDANGER has devices listed in EUDAMED (33 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LANDANGER's devices fall under?
Among its 50 most recently registered devices, the classes recorded for LANDANGER's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from LANDANGER in the registry?
The most recently registered devices listed for LANDANGER include LANDANGER O611842, LANDANGER E503005, DELACROIX-CHEVALIER DC83211-44 and DELACROIX-CHEVALIER DC80234-36.
Which FDA establishments are linked to LANDANGER?
1 FDA establishment is linked to LANDANGER in the registry; they are listed on the company page.