Steinway Instrument Co., Inc.
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- Devices
- 1
What Steinway Instrument Co., Inc. makes
Steinway Instrument Co., Inc. manufactures the Steinway Micro-Kerato-Trephine, a device used in corneal surgery for precise trephination of the cornea, typically for procedures like corneal transplants or refractive surgeries.
The company’s portfolio is regulated under FDA’s Class I device classification, with the Steinway Micro-Kerato-Trephine listed via a 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Steinway Micro-Kerato-Trephine Ref K843646
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Steinway Instrument Co., Inc. have in the registry?
The registry currently lists 1 device for Steinway Instrument Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Steinway Instrument Co., Inc.'s devices?
Among its 1 most recently registered device, Steinway Instrument Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Steinway Instrument Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Steinway Instrument Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Steinway Instrument Co., Inc. in the registry?
The most recently registered devices listed for Steinway Instrument Co., Inc. include STEINWAY MICRO-KERATO-TREPHINE.