Ruggles Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Ruggles Corp. makes
Ruggles Corp. makes trans-oral depth gauges, laminectomy rogeurs, titanium mesh, Zeppelin instruments, and multiple nonpowered neurosurgical instruments.
These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Trans-Oral Depth Gauge Ref K893415
Regimes: 510(k) Registry: 510(k)Laminectomy Rogeur Ref K902819
Regimes: 510(k) Registry: 510(k)Titanium Mesh Ref K903485
Regimes: 510(k) Registry: 510(k)Zeppelin Instruments Ref K902850
Regimes: 510(k) Registry: 510(k)Multiple Nonpowered Neurosurgical Instrument Ref K902818
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ruggles Corp. have in the registry?
The registry currently lists 5 devices for Ruggles Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ruggles Corp.'s devices?
Among its 5 most recently registered devices, Ruggles Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Ruggles Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Ruggles Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ruggles Corp. in the registry?
The most recently registered devices listed for Ruggles Corp. include TRANS-ORAL DEPTH GAUGE, LAMINECTOMY ROGEUR, TITANIUM MESH and ZEPPELIN INSTRUMENTS.