# Allure Spine LLC

- Location (FDA's records): Charlotte, NC
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: MNH (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- U&I Corporation: 1 (https://510kreport.com/company/u-i)
- U&I Corp., America: 1 (https://510kreport.com/company/u-i-america)
- Altiva Corp.: 1 (https://510kreport.com/company/altiva)
- Buckman Co., Inc.: 1 (https://510kreport.com/company/buckman)
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)

## Firms that cite its devices most
- Captiva Spine, Inc.: 1 (https://510kreport.com/company/captiva-spine)

## Its most-cited devices
- K100956: Spondy Spinal Fixation System (2010), cited by 1

## Recent decisions
- K100956: Spondy Spinal Fixation System (Jul 9, 2010)

Source page: https://510kreport.com/company/allure-spine