# Scholten Surgical Instruments, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 8 (1985–2007): 8 510(k) clearances
- Product codes: JEB (1), GAD (1), GEN (1), DTB (1), IZI (1), FOX (1), BWN (1), DWZ (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
- K072051: Novatome, Model: SU101-50 (Oct 3, 2007)
- K900405: Scholten Frame (Mar 1, 1990)
- K852331: Sys, Angiographic, Single-or BI-Plane Radiographic (Aug 1, 1986)
- K852119: Temporary Pacemaker Ground Wire (Sep 15, 1985)
- K852120: Forceps, Biopsy (Non Rigid) (Jul 2, 1985)
- K852332: Table Accessories, Operating Room (Jul 2, 1985)
- K852330: Retractor, Surgical (Jun 27, 1985)
- K852329: Stand, Operating Room (Jun 14, 1985)

Source page: https://510kreport.com/company/scholten-surgical-instruments