CPC SOLUTIONS

FDA Device Registration & Listing · Karmiel Northern, IL · Registration 3011167030

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3011167030
FEI Number
3011167030
Entity Name
CPC SOLUTIONS
City/State/Country
Karmiel Northern, IL
Establishment Address
HaNapah St 18, Karmiel Northern 2165316, IL
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CPC Solutions (Owner Number: 10095346)
Owner / Operator Contact Address
HaNapah St 18, Karmiel, IL-Z 2165316, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

N9+

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DQD Stethoscope, Electronic Cardiovascular Class 2 870.1875 2026-03-02
DQA Oximeter Cardiovascular Class 2 870.2700 2026-03-02
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2026-03-02

Official Correspondent

Shimon Vaknin

US Agent Details

Isaac Elkah Business: Preferred Depot Email: Sagi@Nonagon-Care.com Phone: (844) 7702727

Related Public Records

Same Entity

CPC Solutions
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K771506 Swartz Medical Equipment STETHOSCOPE 1977-08-26
K082528 Noble Anesthesia-Air, Inc. SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM 2009-03-06
K903523 Hewlett-Packard Co. HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE 1990-10-23
K973147 Nellcor Puritan Bennett, Inc. NPB-295 PULSE OXIMETER 1997-11-14
K231243 Guangdong Genial Technology Co., Ltd. Finger Clip Pulse Oximeter 2023-10-31

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0020-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
Z-0023-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
Z-0028-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
Capnostream20 (US) M, Part Number CS08653
Z-0029-2019 Oridion Medical 1987 Ltd. Har Hotzvim Industrial 2
Capnostream20 (US) M W/PRINTER, Part Number CS08659

Similar Registrations

Registration Number Establishment Name Location
3018117676 SPARROW ACOUSTICS INC. Lucasville Nova Scotia, CA
3017394506 SMARTSOUND CORPORATION Gangnam District Seoul, KR
3015134086 TECAN CDMO SOLUTIONS PN SDN. BHD. Penang Pulau Pinang, MY
8010482 RUDOLF RIESTER GMBH JUNGINGEN Baden-Wurttemberg, DE
3004582233 TEAM PRECISION PUBLIC COMPANY LIMITED Tanyaburi Pathum Thani, TH
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011167030. Last updated year: 2026. Please use registration number 3011167030 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.