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FDA 510(k)

NovoFlow Reinforced Ureteral Stent

K-Number: K213186 · 2022-02-16

ApplicantColoplast Corp.
Decision Date2022-02-16
Product CodeFAD
Advisory CommitteeGU
DecisionUnknown

Device Summary

NovoFlow Reinforced Ureteral Stent is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast Corp.. It received FDA 510(k) clearance on 2022-02-16 under 510(k) number K213186. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NovoFlow Reinforced Ureteral Stent?

NovoFlow Reinforced Ureteral Stent is a medical device that received FDA 510(k) clearance on 2022-02-16. The listed applicant is Coloplast Corp.. The 510(k) number is K213186.

When did NovoFlow Reinforced Ureteral Stent receive FDA 510(k) clearance?

NovoFlow Reinforced Ureteral Stent received FDA 510(k) clearance on 2022-02-16, under 510(k) number K213186.

Who is the listed applicant for NovoFlow Reinforced Ureteral Stent?

The FDA 510(k) record lists Coloplast Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NovoFlow Reinforced Ureteral Stent?

The FDA product code for NovoFlow Reinforced Ureteral Stent is FAD.

Other records listing Coloplast Corp. as applicant

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Related Devices (Code: FAD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251890Disposable Ureteral StentsZhejiang Chuangxiang Medical Technology Co., Ltd.K251469Endura™ Ureteral Stent and Stent SetCathegenix (Xiamen) Co., Ltd.K243039Ureteral Stents (AF-D series)Alton (Shanghai) Medical Instruments Co., Ltd.K243830Disposable ureteral stentShenzhen Trious Medical Technology Co., Ltd.K250824Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDrive Steerable Ureteral Stent Set; Contour Ureteral Stent; Contour SureDrive Steerable Ureteral Stent Set; Contour VL Variable Length Ureteral Stent; Contour VL SureDrive Steerable Ureteral Stent Set; Polaris Ultra Ureteral Stent; Polaris Loop Ureteral Stent; Tria Firm Ureteral Stent; Tria Soft Ureteral Stent; Percuflex Urinary Diversion Stent SetBoston Scientific CorporationK232920RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmUreteral Stent Company

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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