# Rexton, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 21 (1983–1997): 21 510(k) clearances
- Product codes: ESD (21)
- 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
- K970537: Rexton Model 48 and 49PP (Mar 28, 1997)
- K964451: Piccolo K-Amp VC+, Piccolo P-A1, Piccolo P-AO and Piccolo Atc (Nov 27, 1996)
- K960295: Long Life RX-12 (Mar 22, 1996)
- K954922: Rexton's Horizion Family of Multiple Situation, Single Channel Programmbale Instruments (Jan 17, 1996)
- K953770: Rexton Mini-Primo Plus, PP142, D.C .H.I. Family (Sep 18, 1995)
- K950451: M-29 PP-PC, M-29 PP-O/PC (Mar 21, 1995)
- K944851: Micro Mini Primo Agc, Micro-Mini Primo S-Agc (Feb 22, 1995)
- K944777: Orion PPM, PP, PP-D (Dec 30, 1994)

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