# Sarstedt, Inc.

- Location (FDA's records): Newton, NC
- FDA decisions: 7 (1992–2023): 7 510(k) clearances
- Names in FDA's records: Sarstedt, Inc. (6); Sarstedt AG & CO KG (1)
- Product codes: JKA (1), FMK (1), FPA (1), JSM (1), FMI (1), KHE (1), PJE (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
- K222801: Safety Lancet (Jan 25, 2023)
- K051019: Safety Needle (Jul 25, 2005)
- K032150: Safety-Multifly (Sep 12, 2003)
- K031359: S-Monovette Edta K2-Gel (Sep 12, 2003)
- K024237: Urine Monovette Boric Acid (Apr 14, 2003)
- K003382: Sarstedt Needle Protector (Mar 30, 2001)
- K913622: Hemoplus (Jan 31, 1992)

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