Ninenovo Blood Oxygen Ring (BORMB-01-6,BORMB-01-7,BORMB-01-8,BORMB-01-9,BORMB-01-10,BORMB-01-11,BORMB-01-12,BORMB-01-13,BORMB-01-14)— 510(k) K260490

Substantially Equivalent

Shenzhen Ninenovo Technology Limited

FDA 510(k) clearance K260490 for Ninenovo Blood Oxygen Ring (BORMB-01-6,BORMB-01-7,BORMB-01-8,BORMB-01-9,BORMB-01-10,BORMB-01-11,BORMB-01-12,BORMB-01-13,BORMB-01-14), Substantially Equivalent on 2026-10-02. Applicant: Shenzhen Ninenovo Technology Limited. Device class: 2.

Summary

The Ninenovo Blood Oxygen Ring is a ring-format device from Shenzhen Ninenovo Technology, cleared in nine sizes or variants, BORMB-01-6 through BORMB-01-14. Product code DQA is oximeters.

Class II, 21 CFR 870.2700. The Anesthesiology review panel handled it as a Traditional 510(k); the record lists Cardiovascular as the classification panel.

Ninenovo filed from Shenzhen, China. Review took 231 days (February 13 to October 2, 2026).

Clearance details

Applicant
Shenzhen Ninenovo Technology Limited
Product code
Product code DQA
Device class
Class 2
Regulation
21 CFR 870.2700
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shenzhen, CN
Download summary PDFView on FDA.gov ↗

Recent devices under product code DQA

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Adverse events under product code DQA

product code DQA
Death
66
Malfunction
2,867
Other
1
Total
2,934

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.