Medmark, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Medmark, Inc. makes
Medmark, Inc. manufactures the Model #520/525 Emergency/Recovery Stretcher, a mobility device designed for patient transport and repositioning, and the #157 Exam Light, a handheld light source for clinical examinations.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. Medmark, Inc. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Model #520/525 Ed/Recovery Stretcher Ref K894987
Regimes: 510(k) Registry: 510(k)#157 Exam Light Ref K893949
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medmark, Inc. have in the registry?
The registry currently lists 3 devices for Medmark, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medmark, Inc.'s devices?
Among its 3 most recently registered devices, Medmark, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Medmark, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medmark, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medmark, Inc. in the registry?
The most recently registered devices listed for Medmark, Inc. include POWDER FREE, NON-STERILE, LATEX EXAMINATION GLOVES, MODEL #520/525 ED/RECOVERY STRETCHER and #157 EXAM LIGHT.