Maxiflex, LLC
Country not established
Maxiflex, LLC is a medical device manufacturer, with 73 devices listed in FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 73
Registry facts
- Registries
- FDA GUDID 73
- Device classes
- FDA Class II 73
- Identifiers
- DUNS 198887072
What Maxiflex, LLC makes
MaxiFlex, LLC manufactures flexible fiberoptic ureteroscopes and reusable and single-use beam guides designed for urogenital surgical laser systems. These devices are intended for procedures involving the ureter and urinary tract, including lithotripsy and tissue ablation. The ureteroscopes enable visualisation and access to narrow or complex anatomical pathways, while the laser beam guides direct energy delivery during minimally invasive surgeries.
The company’s products are classified as Class II medical devices under US regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for use within the United States, adhering to applicable regulatory standards for surgical and diagnostic instruments.
Catalogue
Search and filter all 73 devicesShowing 1-50 of 73
Company details
- DUNS number
- 198887072
Frequently asked questions
How many devices does MAXIFLEX, LLC have in the registry?
The registry currently lists 73 devices for MAXIFLEX, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MAXIFLEX, LLC's devices?
Among its 50 most recently registered devices, MAXIFLEX, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do MAXIFLEX, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for MAXIFLEX, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MAXIFLEX, LLC in the registry?
The most recently registered devices listed for MAXIFLEX, LLC include MaxiFlex Holmium Laser Fiber MF 1000BH C, MaxiFlex Holmium Laser Fiber MF 600BH D R, SemiFlex Scope MF-ENDO 55 LU E and SemiFlex Scope MF-ENDO 55 E.