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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
LinkedIn
—
Facebook
—
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
DeviceModel / ReferenceRegistriesClassStatus
Blue Diamond NCBD-3075
FDA UDI
Class IIActive
Blue Diamond NCBD-2540
FDA UDI
Class IIActive
ActivaTek Ionto4 Butterfly NC89378
FDA UDI
Class IIActive
Blue Diamond NCBD-30100
FDA UDI
Class IIActive
Norco Iontophoresis Medium & Butterfly Sample SA89178
FDA UDI
Class IIActive
Blue Diamond NCBD-2575
FDA UDI
Class IIActive
Exacta Finger Pulse Oximeter NC87031
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Cloth NC89233
FDA UDI
Class IIActive
Blue Diamond NCBD-2560
FDA UDI
Class IIActive
Blue Diamond NCBD-45125
FDA UDI
Class IIActive
Blue Diamond NCBD-25125
FDA UDI
Class IIActive
Norco NC89481
FDA UDI
Class IIActive
Blue Diamond NCBD-3040
FDA UDI
Class IIActive
Blue Diamond NCBD-1613
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Cloth NC89231
FDA UDI
Class IIActive
ActivaTek Ionto4 Kit NC89377
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89282
FDA UDI
Class IIActive
Blue Diamond NCBD-25100
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89279
FDA UDI
Class IIActive
Blue Diamond NCBD-2550
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89285
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89284
FDA UDI
Class IIActive
Blue Diamond NCBD-2530
FDA UDI
Class IIActive
ActivaTek Ionto4 Kit NC89375
FDA UDI
Class IIActive
Blue Diamond NCBD-2513
FDA UDI
Class IIActive
Blue Diamond NCBD-2213
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Cloth NC89234
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89281
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Cloth NC89209
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89287
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Cloth NC89235
FDA UDI
Class IIActive
Blue Diamond NCBD-3050
FDA UDI
Class IIActive
Blue Diamond NCBD-3060
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89278
FDA UDI
Class IIActive
ActivaTek Ionto4 Kit NC89376
FDA UDI
Class IIActive
Blue Diamond NCBD-2013
FDA UDI
Class IIActive
Blue Diamond NCBD-1813
FDA UDI
Class IIActive
Blue Diamond NCBD-3030
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Foam NC89283
FDA UDI
Class IIActive
Norco Iontophoresis Large Sample SA89252B
FDA UDI
Class IIActive
Norco Multi-Use Electrode, Cloth NC89232
FDA UDI
Class IIActive
Blue Diamond NCBD-40100
FDA UDI
Class IIActive
Comfort Cool Thumb CMC Restriction Splint, RM+ NC79559
EUDAMED
Class IActive
Exacta Devore Pocket Goniometer NC70115
EUDAMED
Class IActive
Norco Ortho Foam PIP Extension Orthotic, Small NC85501-2
EUDAMED
Class IActive
Air Putty(R) NC52415-60
EUDAMED
Class IActive
Progress Individual Finger Separator NC25342
EUDAMED
Class IActive
Progress Ultra-Ortho, Medium, Right Multi-purpose Orthotic NC25565
EUDAMED
Class IActive
Comfort Cool Thumb CMC Restriction Splint, LL NC79566
EUDAMED
Class IActive
Norco Ortho-Foam Terminal PIP Extension Orthotic, Sm. NC85507-2
EUDAMED
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

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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.

DateRecall No.ClassStatusReason
Aug 18, 2023Z-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, 2021Z-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, 2021Z-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