# Brm Extremities

- Location (FDA's records): Civate, IT
- FDA decisions: 4 (2020–2023): 4 510(k) clearances
- Names in FDA's records: Brm Extremities (2); Brm Extremities Srl (2)
- Product codes: HWC (2), KWH (1), KYJ (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 1 (1 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
- Ascension Orthopedics, Inc.: 2 (https://510kreport.com/company/ascension-orthopedics)
- In2bones USA, LLC: 1 (https://510kreport.com/company/in2bones-usa)
- In2bones Sas: 1 (https://510kreport.com/company/in2bones)
- Sutter Biomedical, Inc.: 1 (https://510kreport.com/company/sutter-biomedical)
- Sutter Corp.: 1 (https://510kreport.com/company/sutter)
- Ortho Solutions UK, Ltd.: 1 (https://510kreport.com/company/ortho-solutions-uk)

## Its most-cited devices
- K203773: BRM TOOL Screws (2022), cited by 1

## Recent decisions
- K220142: BRM Digitalis Spacer (Apr 4, 2023)
- K222820: BRM TOOL Screws, BIOPLAN Subtalar Implant (Dec 16, 2022)
- K203773: BRM TOOL Screws (Jan 14, 2022)
- K191966: NewPrim System (Feb 13, 2020)

Source page: https://510kreport.com/company/brm-extremities