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NORTH 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/
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 (408) 776-5000
PRRC Contact: Danielle Abtin
EUDAMED SRN: US-MF-000009087
FDA FEI Number: 1000124207
DUNS Number: —

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Device	Model / Reference	Registries	Class	Status
Norco Compression Gloves	NC53218	EUDAMED	Class I	Active
Self-Adhesive D-Ring Straps with Hook Loop White, 1 x 12 in (10)	NC15280	EUDAMED	Class I	Active
Comfort Cool Thumb CMC Restriction Splint, Bg, LXL	NC79592	EUDAMED	Class I	Active
Norco Elbow/Heel Protectors, MD (PR)	NC58801-2	EUDAMED	Class I	Active
Norco Heavy Compression Gloves	NC55322	EUDAMED	Class I	Active
Norco Dema Grip Gentle Compression Stockinette B Black 2 1/2in x 33 ft	NC42801	EUDAMED	Class I	Active
Progress Elbow Orthosis Olecranon Pad, Youth/Adult	NC25649	EUDAMED	Class I	Active
Spectrum	NC12922	EUDAMED	Class I	Active
Solaris	NC14031-1	EUDAMED	Class I	Active
Norco Compression Gloves	NC53222-B	EUDAMED	Class I	Active
Norco Dema Grip Gentle Compression Stockinette F, Natural 4 in x 33 ft	NC42705	EUDAMED	Class I	Active
Omega Plus	NC13313	EUDAMED	Class I	Active
Comfort Cool Firm D-Ring Wrist Orthosis, LXL	NC52988	EUDAMED	Class I	Active
Comfort Cool D-Ring Thumb/Wrist, LS Wrist Orthosis	NC91252	EUDAMED	Class I	Active
Norco Finger Sleeves, Open, MD	NC53055-3	EUDAMED	Class I	Active
Big-Grip	NC65599	EUDAMED	Class I	Active
Achieva Quik-Knot Exercise Handle (PR) and Clip	NC85081	EUDAMED	Class I	Active
Encore	NC14053-1K	EUDAMED	Class I	Active

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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