# Effortmed, LLC

- Location (FDA's records): Coral Springs, FL
- FDA decisions: 3 (2024–2025): 3 510(k) clearances
- Product codes: NKB (1), ODP (1), KWQ (1)
- 510(k) review time since 2016: median 42 days, against 64 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 2 (0 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
- Artfx Medical: 3 (https://510kreport.com/company/artfx-medical)
- Mikron Makina Sanayi VE Ticaret Ltd. Sti.: 1 (https://510kreport.com/company/mikron-makina-sanayi-ve-ticaret-sti)
- Xtant Medical Holdings, Inc.: 1 (https://510kreport.com/company/xtant-medical-holdings)
- Arftx Medical, LLC: 1 (https://510kreport.com/company/arftx-medical)
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)

## Firms that cite its devices most
- Osteomni, Inc.: 2 (https://510kreport.com/company/osteomni)

## Its most-cited devices
- K243946: EffortMed Spinal Fixation System (2025), cited by 1
- K252686: EffortMed PEEK Cages & Corpectomy Cages (2025), cited by 1

## Recent decisions
- K252686: EffortMed PEEK Cages & Corpectomy Cages (Nov 21, 2025)
- K243946: EffortMed Spinal Fixation System (Jan 15, 2025)
- K240935: ARENAL Anterior Cervical Plate System (May 17, 2024)

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