# Xre Corp.

- Location (FDA's records): Littleton, MA
- FDA decisions: 20 (1977–1997): 20 510(k) clearances
- Product codes: IZI (10), IXR (3), JAA (2), IZZ (1), GDC (1), IZW (1), IYB (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K973744: Unicath SP BI-Plane (Model M269 & M289) (Dec 29, 1997)
- K961193: Full Frame Zoom System (Jun 17, 1996)
- K960998: Xre Collimator (Apr 3, 1996)
- K945449: Unicath Llu Angiographic System (Feb 27, 1995)
- K936002: Cinemac Qas (Sep 9, 1994)
- K933460: DVFX, Model M256 (Apr 7, 1994)
- K924828: BI-N (Dec 17, 1992)
- K923654: Poly Diagnost CDX (Nov 20, 1992)

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