# Novosci Corp.

- Location (FDA's records): The Woodlands, TX
- FDA decisions: 4 (2004–2007): 4 510(k) clearances
- Names in FDA's records: Novosci Corp. (3); Novosci, Inc. (1)
- Product codes: KFM (1), MSD (1), DTL (1), MPB (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- Medical Components, Inc.: 2 (https://510kreport.com/company/medical-components)
- Medcomp: 1 (https://510kreport.com/company/medcomp)
- Kendall Healthcare Products Co. Div.Of Tyco Health: 1 (https://510kreport.com/company/kendall-healthcare-products-co-div-of-tyco-health)
- Kendall: 1 (https://510kreport.com/company/kendall)

## Firms that cite its devices most
- Foshan Nanhai Bai HE Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/foshan-nanhai-bai-he-medical-technology)

## Its most-cited devices
- K063355: D-Line Catheter ST, Double Lumen ST; Extra Flow (2007), cited by 1

## Recent decisions
- K072499: Novoflo Catheter LT (Oct 30, 2007)
- K063355: D-Line Catheter ST, Double Lumen ST; Extra Flow (Jul 27, 2007)
- K033270: Novosci Ready System, Model RS-200 (Feb 13, 2004)
- K033328: Novosci Tubing and Connectors with Novocoat Treatment (Jan 16, 2004)

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