# Mani, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 4 (2005–2006): 4 510(k) clearances
- Product codes: GAM (1), GAR (1), GAT (1), GAP (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Alcon Laboratories: 2 (https://510kreport.com/company/alcon-laboratories)
- Samyang Corp.: 1 (https://510kreport.com/company/samyang)
- Cp Medical: 1 (https://510kreport.com/company/cp-medical)

## Recent decisions
- K053637: Mani Needle & Suture Pack (Nylon) (May 19, 2006)
- K053638: Mani Needle & Suture Pack (Silk) (May 19, 2006)
- K053636: Mani Needle & Suture Pack (Pga  Absorbable) (Mar 14, 2006)
- K050150: Mani Needle & Suture Pack (Dec 5, 2005)

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