# Vertera, Inc.

- Location (FDA's records): Atlanta, GA
- FDA decisions: 2 (2015–2017): 2 510(k) clearances
- Product codes: MAX (1), ODP (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Eisertech, LLC: 1 (https://510kreport.com/company/eisertech)
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)

## Firms that cite its devices most
- Nu Vasive, Incorporated: 3 (https://510kreport.com/company/nu-vasive)

## Its most-cited devices
- K163506: Coalesce™ (-Straight, -Convex, -Crescent, -Lateral, -Anterior, or -Oblique) Lumbar Interbody Fusion System (2017), cited by 2
- K143685: Hedgehog Cervical Interbody Fusion Device (2015), cited by 1

## Recent decisions
- K163506: Coalesce™ (-Straight, -Convex, -Crescent, -Lateral, -Anterior, or -Oblique) Lumbar Interbody Fusion System (Jun 19, 2017)
- K143685: Hedgehog Cervical Interbody Fusion Device (Sep 23, 2015)

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