Relieva Spin

The Relieva Spin sinus guide catheter tip is a component of the Relieva Spin Sinus Dilation System. It attaches to the distal end of the handle system and helps provide access to the sinus…

Registry build 21.09.26

The Relieva Spin sinus guide catheter tip is a component of the Relieva Spin Sinus Dilation System. It attaches to the distal end of the handle system and helps provide access to the sinus space during diagnostic and therapeutic procedures.

The guide tip is available in three shapes. The complete system combines the tip, handle and a separate balloon catheter, with a sinus guidewire used to reach the target location. Balloon dilation is performed by the balloon catheter rather than the guide tip.

Listed Item

Relieva Spin Balloon Sinuplasty System, M-110C Sinus Guide Catheter TIP, 1 PK

System Application

The system accesses and dilates sinus ostia and spaces associated with the paranasal sinus cavities. In children aged 17 or younger, its dilation indication is limited to the maxillary sinus. Positioning is performed under direct endoscopic visualization.

11manufacturers in China registered for this device type
20catalogue numbers in this listing
13510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Guangdong (4), Jiangsu (3), Zhejiang (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LRC
Manufacturer City Province Registered as Device types
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14
Shenzhen Insighters Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Elite Medtek(Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 9
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Modern Medical Equipment Manufacturing (Qing Yuan) Ltd Qing Yuan Guangdong Contract manufacturer 26
Shenzhen Hugemed Medical Technical Development Co., Ltd. Shenzhen Guangdong Manufacturer 22
Hangzhou Endo Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Jiangsu Yongle Medical Technology Co., Ltd. Taixing Jiangsu Manufacturer 4

Record

Regulatory record for Relieva Spin
Listed by Acclarent, Inc., United States
FDA product code LRC
Device type Instrument, Ent Manual Surgical
Device class Class 1
Regulation 21 CFR 874.4420
Establishment Specification developer, Manufacturer
510(k) K111875
Record published 2016-10-01
Record revised 2024-11-21 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store in a cool, dry place
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for Relieva Spin
Catalogue number Size Status
RS0616MFSZ In distribution
RS0616FZ In distribution
RS0616MFS In distribution
RS0516MFS In distribution
RS0616F In distribution
RSM110Z In distribution
RS0516MFSZ In distribution
RSF70 In distribution
RSM110C In distribution
RS0616M In distribution
RSS0Z In distribution
RSS0 In distribution
RSF70Z In distribution
RS0516M In distribution
RS0516FZ In distribution
RSM110CZ In distribution
RSM110 In distribution
RS0516MZ In distribution
RS0616MZ In distribution
RS0516F In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Instrument, Ent Manual Surgical Karl Storz GmbH & Co. KG 2,062
Fentex Fentex medical GmbH 1,738
Elmed Elmed, Inc. 504
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 441
Evonos Gyrus Acmi, Inc. 291
Millennium Avalign Technologies, Inc. 283
Elmed Incorporated Elmed, Inc. 277
Instrument, Ent Manual Surgical Stryker Leibinger Gmbh & Co. KG 169
Rhinoforce Karl Storz GmbH & Co. KG 112
Surtex Surtex Instruments Ltd 85
Kerrison sphenoid punch Spiggle & Theis Medizintechnik Gmbh 82
Gyrus Acmi Gyrus Acmi, Inc. 78

Showing 12 of 661. All products under Instrument, Ent Manual Surgical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201115 2020-08-27
K190525 2019-05-03
K171687 2017-09-05
K161698 2016-10-24
K153341 2016-02-12
K143541 2015-04-22
K150172 2015-04-07
K140160 2014-02-20
K120280 2012-11-05
K111875 2011-10-11
K111254 2011-08-22
K061903 2006-08-18
K052198 2005-08-31

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2006-01-20 Not classified Other Device sterility may be compromised as evidenced by a loss of package integrity. 149 units 2006-05-11

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer