# Adam Spence Corp.

- Location (FDA's records): Wall, NJ
- FDA decisions: 3 (1995–1999): 3 510(k) clearances
- Product codes: DQO (2), DYB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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
- Daig Corp.: 1 (https://510kreport.com/company/daig)

## Recent decisions
- K983940: EZ-Intro Percutaneous Catheter Sheath, EZ-Intro Vessel Dilator (Jul 15, 1999)
- K955111: Maxi-Torque Plus Angiographic Catheter (Jan 31, 1996)
- K950855: Ase Maxi-Torque, Supple Flex Angiographic Catheters (May 30, 1995)

Source page: https://510kreport.com/company/adam-spence