Congruence Medical Solutions, LLC
United Statesfrom the FDA registration address FDA FEI 3014623935
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Congruence Medical Solutions, LLC makes
Congruence Medical Solutions manufactures precision microliter dosing syringes in multiple volumes, including 9, 20, 25, 37.5, 50, and 100 microliters. These devices are designed for accurate liquid dispensing in medical and laboratory applications, supporting tasks requiring fine volumetric control.
The company’s microliter dosing syringes are classified as Class II medical devices under FDA regulations and are listed via 510(k) premarket notifications. The portfolio is authorised for use in the United States, where the manufacturer is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3014623935
- Address
- 3000 Falls Rd Ste 200a, Baltimore, MD, 21211
Frequently asked questions
How many devices does Congruence Medical Solutions, LLC have in the registry?
The registry currently lists 1 device for Congruence Medical Solutions, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Congruence Medical Solutions, LLC's devices?
Among its 1 most recently registered device, Congruence Medical Solutions, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Congruence Medical Solutions, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Congruence Medical Solutions, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Congruence Medical Solutions, LLC in the registry?
The most recently registered devices listed for Congruence Medical Solutions, LLC include Microliter Dosing Syringe (9, 20, 25, 37.5, 50 and 100 microliter models).