# Us Medical Innovations, LLC

- Location (FDA's records): Takoma Park, MD
- FDA decisions: 5 (2011–2024): 5 510(k) clearances
- Product codes: GEI (3), GCJ (1), OAB (1)
- 510(k) review time since 2016: median 107 days, against 103 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 12 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Erbe USA, Inc.: 4 (https://510kreport.com/company/erbe-usa)
- Valleylab, Inc.: 2 (https://510kreport.com/company/valleylab)
- Canady Technology, LLC: 1 (https://510kreport.com/company/canady-technology)
- Aaron Medical Industries: 1 (https://510kreport.com/company/aaron-medical-industries)
- I.C Medical, Inc.: 1 (https://510kreport.com/company/i-c-medical)
- Novare Surgical Systems, Inc.: 1 (https://510kreport.com/company/novare-surgical-systems)

## Its most-cited devices
- K100669: Canady Plasma Electrosurgical Unit Series with Accessory Probes and Blades (2011), cited by 1
- K192124: Canady Plasma SMART XL-1000 Electrosurgical Generator with Accessories (2019), cited by 1

## Recent decisions
- K240297: Canady Helios Cold Plasma™ XL-1000CP™ Ablation System (XL-1000CPSYS) (May 3, 2024)
- K212736: Canady Flex RoboWrist (Nov 22, 2022)
- K192124: Canady Plasma SMART XL-1000 Electrosurgical Generator with Accessories (Nov 21, 2019)
- K113500: Canady Vieira Hybrid Plasma Scalpel (Dec 9, 2011)
- K100669: Canady Plasma Electrosurgical Unit Series with Accessory Probes and Blades (Apr 6, 2011)

Source page: https://510kreport.com/company/us-medical-innovations