AIRvance™

Bone Screw 76353200M Airvance SYS Rohs

Registry build 21.09.26
8manufacturers in China registered for this device type
5catalogue numbers in this listing
2510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Guangdong (6), Zhejiang (1), Fujian (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LRK
Manufacturer City Province Registered as Device types
Modern Dental Laboratory (DG) Co., Ltd. Dongguan Guangdong Contract manufacturer 15
Xiamen Yizhou IMP. & EXP. Co., Ltd. Xiamen Fujian Contract manufacturer 10
Dongguan Yiyao Science & Technology Development Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Dongyang City Yonoel Outdoor Products Co., Ltd. Dongyang Zhejiang Contract manufacturer 32
Digital Dental Depot Zhuhai Guangdong Contract manufacturer 17
Shenzhen Sany Pioneer Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Zhuhai DS Dental Technology Co., Ltd. Zhuhai Guangdong Manufacturer 8
Shenzhen Kesite Digital Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 4

Record

Regulatory record for AIRvance™
Listed by Medtronic Xomed, Inc., United States
FDA product code LRK
Device type Device, Anti-Snoring
Device class Class 2
Regulation 21 CFR 872.5570
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K981677
Record published 2016-04-22
Record revised 2025-04-29 (version 4)

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
Storage Storage environment temperature -40 to 60 °C
Distribution end date 2023-12-06

Catalogue Numbers

Catalogue numbers for AIRvance™
Catalogue number Size Status
76310200M Withdrawn
76353200M Withdrawn
76353200M Withdrawn
76310200M Withdrawn
76353200M Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Emerald Herbst Island Dental LAB DBA Emerald Dental LAB 141
EMA The Myerson Company Limited 94
Apnea Guard Advanced Brain Monitoring, Inc. 32
SML Selane Products, Inc. 32
SomnoDent Avant Somnomed, Ltd. 11
Itus Mouthguardz Shinrin-Yoku Traders LLC 8
Virtus Somnomed, Ltd. 7
Silent Nite Sleep Appliance with Glidewell Hinge Prismatik Dentalcraft, Inc. 7
ZQuiet S.A. Sleeping Well, LLC 6
Zyppah A.M.A. Plastics 6
Anti-snoring, restoration Modern Dental Laboratory (DG) Co., Ltd. 4
EMA Custom The Myerson Company Limited 4

Showing 12 of 209. All products under Device, Anti-Snoring

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K122391 2013-01-10
K110623 2012-02-10

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of AIRvance™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Medtronic Xomed, Inc. 510(k) number 2009-07-27 Not classified Labeling mix-ups Medtronic Xomed, Inc. is recalling the Repose Bone Screw System product and Bone Screw product due to improper labeling. The labeling for the Repose System was inadvertently placed on the Repose Screw and vice versa. 7 2010-03-15
Medtronic Xomed, Inc. 510(k) number 2009-07-27 Not classified Labeling mix-ups Medtronic Xomed, Inc. is recalling the Repose Bone Screw System product and Bone Screw product due to improper labeling. The labeling for the Repose System was inadvertently placed on the Repose Screw and vice versa. 13 2010-03-15

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