Data / Medical devices / Italy / Ri.mos. SRL
Ri.mos. SRL: FDA-registered device maker in MIRANDOLA (MO) Modena, Italy, 2 510(k) clearances
Ri.mos. SRL is registered with the FDA (registration 9614868) in MIRANDOLA (MO) Modena, Italy. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated October 5, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9614868
- FEI number
- 3002926090
- Address
- Via Manuzio 15, MIRANDOLA (MO) Modena, Italy, 41037
- Owner or operator
- Ri.Mos. Srl (10094582)
- Roles
- Manufacturer
- First device listed
- December 9, 2025
- Registered through
- 2026
- Brand names listed
- MESORAM® MULTI-INJECTORS WITHOUT NEEDLES - CIRCULAR WITH SEVEN CONNECTIONS - REF. 710105, MESORAM® Circular Multi-injector with five hypodermic needles 27G - 0,40 X 4 mm - REF. 710203, MESORAM® Circular Multi-injector with five hypodermic needles 27G - 0,40 X 6 mm - REF. 710204, MESORAM® Circular Multi-injector with five hypodermic needles 30G - 0,30 X 4 mm - REF. 710211, MESORAM® Circular Multi-injector with five hypodermic needles 30G - 0,30 X 6 mm - REF. 710212, MESORAM® Circular Multi-injector with seven hypodermic needles 27G - 0,40 X 4 mm - REF. 710207, MESORAM® Circular Multi-injector with seven hypodermic needles 27G - 0,40 X 6 mm - REF. 710208, MESORAM® Circular Multi-injector with seven hypodermic needles 30G - 0,30 X 4 mm - REF. 710216 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 5, 2023 | K230070 | MESORAM® Hypodermic Needle (710301); MESORAM® Hypodermic Needle (710302); MESORAM® Hypodermic Needle (712305); MESORAM® Hypodermic Needle (712315); MESORAM® Hypodermic Needle (710303); MESORAM® Hypodermic Needle (710307); MESORAM® Hypodermic Needle (710306); MESORAM® Hypodermic Needle (712308); MESORAM® Hypodermic Needle (712318); MESORAM® Hypodermic Needle (712303); MESORAM® Hypodermic Needle (712307); MESORAM® Hypodermic Needle (712306); MESORAM® Hypodermic Needle (812400); MESORAM® | FMI | Substantially Equivalent | Promamedical, Inc. | accessdata.fda.gov |
| January 19, 2017 | K161255 | meso-relle (AAL34, AAL36, AM30G) | FMI | Substantially Equivalent | Biotekne Srl | accessdata.fda.gov |
Compare with other makers
Updated October 5, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.