Medical Workshop
Country not established
- Devices
- 1
What Medical Workshop makes
Medical Workshop produces ethylene oxide (ETO) sterilization methods specifically for intraocular lenses, ensuring compliance with sterilization protocols for ophthalmic implants.
The company’s portfolio is regulated under the FDA’s 510(k) clearance process, and its devices are listed in the United States. The company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Eto Method - Sterilize Intraocular Lens Ref K761178
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Workshop have in the registry?
The registry currently lists 1 device for Medical Workshop. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Workshop's devices?
Among its 1 most recently registered device, Medical Workshop has devices listed in FDA 510(k) (1 device).
What are the newest devices from Medical Workshop in the registry?
The most recently registered devices listed for Medical Workshop include ETO METHOD - STERILIZE INTRAOCULAR LENS.