INNO HEALTH TECHNOLOGY CO., LTD.
智順科技股份有限公司
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1Plants
6Certifications
3Patents
< NT$20MRevenue band (est.)
- Unified Business No.
- 70657296
- Industry
- Other Manufacturing (2,432)
- Main products
- Medical devices & supplies (878)
- Location
- NO.36, JINGKE 8TH RD., NANTUN DIST., TAICHUNG CITY, TAIWAN (R.O.C.)
Taichung City (17,121) · Nantun Dist. (433) - Listing
- Not publicly issued (84,625)
- Organisation type
- Company Limited by Shares
- Representative
- Chiang Chih-cheng
- Phone
- 04-35077450
- Exporter
- Yes — registered with the Trade Administration
- Annual revenue band
- < NT$20M estimated
- Ownership
- Group subsidiary / corporate-held · Hsin Chieh Tou Tzu Co., Ltd.
- North American market
- FDA 510(k) clearance FDA medical device registration
- Representative tenure
- In office since at least 2013 (13+ years)
- Compliance record
- FDA import refusal: 2 product(s), latest 2021-01-20
Certifications 6
- Medical device license (Class I) (1,430)Official registry Valid until 2027-02-17 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2017-04-11 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2016-07-29 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class II) (794)Official registry Valid until 2031-05-17 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class II) (794)Official registry Valid until 2029-11-26 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class II) (794)Official registry Valid until 2029-12-01 · Taiwan Food and Drug Administration (TFDA)
Patents 3
- 2025 Acupuncture device with acupoint finding and artificial intelligence
- 2021 Bidirectional diagnostic and treatment device connectable to blood pressure measurement
- 2021 Seated lumbar traction and intervertebral disc massage equipment
North American market evidence 4
- FDA 510(k) clearance K091933 2010-04-02
ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01 - FDA 510(k) clearance K051197 2006-03-28
ACULIFE, MODEL SMW-01 - FDA medical device registration 3003755374 2001-03-29 – 2020-08-31
Stimulator, Electro-Acupuncture; Massager, Therapeutic, Manual; Collector, Urine, (And Accessories) For Indwelling Catheter and more (8) - FDA import refusal 3003755374 2020-08-21 – 2021-01-20
REAGENT, CORONAVIRUS SEROLOGICAL; CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Public registers of the US FDA, the FCC and Health Canada, matched on the registered English name. An FDA import refusal is a negative record, but also shows goods actually shipped to the US. The FCC dataset ends in 2021.
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