Heraeus, Inc.
Country not established
- Devices
- 1
What Heraeus, Inc. makes
Heraeus, Inc. makes the ENDO L 300 LIGHT, an illuminating wound retractor used in endoscopic procedures.
This device is listed in the FDA 510(k) registry and is classified as a Class II medical device; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Endo L 300 Light, Illuminating Wound Rectractor Ref K853460
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heraeus, Inc. have in the registry?
The registry currently lists 1 device for Heraeus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heraeus, Inc.'s devices?
Among its 1 most recently registered device, Heraeus, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Heraeus, Inc. in the registry?
The most recently registered devices listed for Heraeus, Inc. include ENDO L 300 LIGHT, ILLUMINATING WOUND RECTRACTOR.