# Ri Mos. S.R.L.

- Location (FDA's records): Concord, MA
- FDA decisions: 4 (1999–1999): 4 510(k) clearances
- Product codes: HHK (2), HIB (1), HEE (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Welch Allyn, Inc.: 1 (https://510kreport.com/company/welch-allyn)

## Its most-cited devices
- K991895: Rampipella, Singe Port (720196) & Wedge-Shaped Port (720217) (1999), cited by 1

## Recent decisions
- K992926: Ginram Endocic Single Oval Port (Model NO. 720195) (Oct 26, 1999)
- K991895: Rampipella, Singe Port (720196) & Wedge-Shaped Port (720217) (Aug 12, 1999)
- K991827: Ginram Specuvag, Ginram Specuvag as, Ginram Cuscovag, Models 720101, 720102, 720103, 720179, 720227, 720043 (Jul 19, 1999)
- K983897: Cervical Anesthesia Needle, Contracervical Anesthesia Needle, Model #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G (Feb 1, 1999)

Source page: https://510kreport.com/company/ri-mos