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Sign in to claim this brandNORTH COAST MEDICAL, INC.
United States·US-MF-000009087
Last updated September 17, 2026
Information
- Country
- United States
- Address
- Suite #110, 135 East Main Avenue, Morgan Hill, California, United States
- Website
- www.ncmedical.com/
- —
- —
- [email protected]
- Phone
- +1 (408) 776-5000
- PRRC Contact
- Danielle Abtin
- EUDAMED SRN
- US-MF-000009087
- FDA FEI Number
- 1000124207
- DUNS Number
- —
Catalogue (669)
Page 1 of 14| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Blue Diamond | NCBD-3075 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2540 | FDA UDI | Class II | Active |
| ActivaTek Ionto4 Butterfly | NC89378 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-30100 | FDA UDI | Class II | Active |
| Norco Iontophoresis Medium & Butterfly Sample | SA89178 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2575 | FDA UDI | Class II | Active |
| Exacta Finger Pulse Oximeter | NC87031 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Cloth | NC89233 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2560 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-45125 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-25125 | FDA UDI | Class II | Active |
| Norco | NC89481 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-3040 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-1613 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Cloth | NC89231 | FDA UDI | Class II | Active |
| ActivaTek Ionto4 Kit | NC89377 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89282 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-25100 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89279 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2550 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89285 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89284 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2530 | FDA UDI | Class II | Active |
| ActivaTek Ionto4 Kit | NC89375 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2513 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2213 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Cloth | NC89234 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89281 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Cloth | NC89209 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89287 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Cloth | NC89235 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-3050 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-3060 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89278 | FDA UDI | Class II | Active |
| ActivaTek Ionto4 Kit | NC89376 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-2013 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-1813 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-3030 | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Foam | NC89283 | FDA UDI | Class II | Active |
| Norco Iontophoresis Large Sample | SA89252B | FDA UDI | Class II | Active |
| Norco Multi-Use Electrode, Cloth | NC89232 | FDA UDI | Class II | Active |
| Blue Diamond | NCBD-40100 | FDA UDI | Class II | Active |
| Comfort Cool Thumb CMC Restriction Splint, RM+ | NC79559 | EUDAMED | Class I | Active |
| Exacta Devore Pocket Goniometer | NC70115 | EUDAMED | Class I | Active |
| Norco Ortho Foam PIP Extension Orthotic, Small | NC85501-2 | EUDAMED | Class I | Active |
| Air Putty(R) | NC52415-60 | EUDAMED | Class I | Active |
| Progress Individual Finger Separator | NC25342 | EUDAMED | Class I | Active |
| Progress Ultra-Ortho, Medium, Right Multi-purpose Orthotic | NC25565 | EUDAMED | Class I | Active |
| Comfort Cool Thumb CMC Restriction Splint, LL | NC79566 | EUDAMED | Class I | Active |
| Norco Ortho-Foam Terminal PIP Extension Orthotic, Sm. | NC85507-2 | EUDAMED | Class I | Active |
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Aug 18, 2023 | Z-0125-2024 | — | open, classified | The thumb strap of the wrist and thumb orthosis may contain latex that is not declared in the product labeling. |
| Aug 27, 2021 | Z-2582-2021 | — | open, classified | Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health |
| Aug 27, 2021 | Z-2583-2021 | — | open, classified | Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health |