Cimarron Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Cimarron Instruments, Inc. makes
Cimarron Instruments, Inc. manufactures surgical tools including a bipolar coagulator for tissue sealing, disposable skin retractors for wound exposure, and electrosurgical units like the Cimarron 1000 series and Dual-Trol for controlled tissue cutting and coagulation.
The company’s devices are classified as Class II under FDA regulations and are authorised via 510(k) clearance. They are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Pao Bipolar Coagulator Ref K840545
Regimes: 510(k) Registry: 510(k)Disposable Skin Retractor Ref K801151
Regimes: 510(k) Registry: 510(k)Cimarron 1000 Or 1000-2 Ref K790293
Regimes: 510(k) Registry: 510(k)Dual-Trol Ref K802972
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cimarron Instruments, Inc. have in the registry?
The registry currently lists 4 devices for Cimarron Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cimarron Instruments, Inc.'s devices?
Among its 4 most recently registered devices, Cimarron Instruments, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cimarron Instruments, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cimarron Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cimarron Instruments, Inc. in the registry?
The most recently registered devices listed for Cimarron Instruments, Inc. include PAO BIPOLAR COAGULATOR, DISPOSABLE SKIN RETRACTOR, CIMARRON 1000 OR 1000-2 and DUAL-TROL.