# Exsomed Corp.

- Location (FDA's records): Aliso Viejo, CA
- FDA decisions: 4 (2019–2022): 4 510(k) clearances
- Names in FDA's records: Exsomed Corp. (2); Exsomed Corporation (2)
- Product codes: HWC (3), HRS (1)
- 510(k) review time since 2016: median 53 days, against 99 for FDA's reviews in the same codes and years (4 of 4 faster)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 5 (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
- Exsomed Holdings Company, LLC: 2 (https://510kreport.com/company/exsomed-holdings)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Gramercy Extremity Orthopeidics, LLC: 1 (https://510kreport.com/company/gramercy-extremity-orthopeidics)

## Firms that cite its devices most
- Dev4: 1 (https://510kreport.com/company/dev4)
- Orthocircle Spine D.B.A. OC Medical Devices: 1 (https://510kreport.com/company/orthocircle-spine-dba-oc-medical-devices)
- Orthopaedic Implant Company: 1 (https://510kreport.com/company/orthopaedic-implant)

## Its most-cited devices
- K183603: INnate Cannulated Screw System (2019), cited by 4
- K201430: InFrame™ Cannulated Fixation System (2020), cited by 1

## Recent decisions
- K220892: ExsoMed INnate NanoTM Lag Screw System (Apr 27, 2022)
- K201430: InFrame™ Cannulated Fixation System (Jun 20, 2020)
- K192473: Exsomed Wrist Plating System (Dec 3, 2019)
- K183603: INnate Cannulated Screw System (Mar 12, 2019)

Source page: https://510kreport.com/company/exsomed