# Osteomed Implantes, Ltda

- Location (FDA's records): Rio Claro - Sp, BR
- FDA decisions: 3 (2015–2016): 3 510(k) clearances
- Product codes: KWQ (1), MNI (1), ODP (1)
- Predicates its devices cite: 21 (0 its own); citations of its devices by later devices: 4 (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
- Depuy Spine, Inc.: 4 (https://510kreport.com/company/depuy-spine)
- Synthes (Usa): 3 (https://510kreport.com/company/synthes-usa)
- Stryker Spine: 3 (https://510kreport.com/company/stryker-spine)
- Spinal Elements, Inc.: 3 (https://510kreport.com/company/spinal-elements)
- Synthes Spine: 2 (https://510kreport.com/company/synthes-spine)
- Biomet Spine: 1 (https://510kreport.com/company/biomet-spine)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Sulzer Spine-Tech: 1 (https://510kreport.com/company/sulzer-spine-tech)

## Firms that cite its devices most
- Nvision Biomedical Technologies, Inc.: 2 (https://510kreport.com/company/nvision-biomedical-technologies)
- Valorus Spine: 1 (https://510kreport.com/company/valorus-spine)
- Aurora Spine, Inc.: 1 (https://510kreport.com/company/aurora-spine)

## Its most-cited devices
- K151553: Anterior Cervical Plate System (2016), cited by 4

## Recent decisions
- K151553: Anterior Cervical Plate System (Feb 10, 2016)
- K143572: Intersomatic Cervical Device - DICOM PEEK, Intersomatic Intervertebral Space Maintenance Device - DIMEI PEEK, Intersomatic Transforaminal - TLIF PEEK (Jun 10, 2015)
- K150294: DPZ Pedicular Fixation System (Jun 5, 2015)

Source page: https://510kreport.com/company/osteomed-implantes