Lavage, Jet

Femoral Canal Brush, Irrigation/Suction with Increased Suction

Registry build 21.09.26
17manufacturers in China registered for this device type
40catalogue numbers in this listing
1510(k) clearance
9recalls on this code

Who Else Makes It

Concentrated in Guangdong (7), Beijing (4), Jiangsu (3). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FQH
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Elite Medtek(Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 9
Dongguan Kaiser Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 7
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Beijing Zksk Technology Co., Ltd. Beijing Beijing Contract manufacturer 38
Dongguan Hong De Medical Plastic Products Co., Ltd. Dongguan Guangdong Contract manufacturer 32
Bothwin (Beijing) Medical Technology Co., Ltd. Beijng Beijing Manufacturer 25
Shenzhen Hugemed Medical Technical Development Co., Ltd. Shenzhen Guangdong Manufacturer 22
Anqing Changfan Medical Instrument Co., Ltd. Anqing Anhui Manufacturer 9
Shenzhen Relish Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 9

Showing 12 of 17. All 17 manufacturers in China registered for Lavage, Jet

Record

Regulatory record for Lavage, Jet
Listed by Stryker GmbH, Switzerland
FDA product code FQH
Device type Lavage, Jet
Device class Class 2
Regulation 21 CFR 880.5475
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-09-23
Record revised 2025-12-03 (version 6)

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
Storage Storage environment temperature -20 to 40 °C; Storage environment humidity 10 to 75 % RH; Storage environment atmospheric pressure 50 to 106 KiloPascal
Packaging Pack of 12, pack of 10, pack of 6
Distribution end date 2017-07-01

Catalogue Numbers

Catalogue numbers for Lavage, Jet
Catalogue number Size Status
0210001000 In distribution
0210017000 In distribution
0210014100 In distribution
0207061000 In distribution
0207064000 In distribution
0207066000 In distribution
0207062000 In distribution
0207053000 In distribution
0210058000 In distribution
0210010000 In distribution
0210005000 In distribution
0210018100 In distribution
0207058000 In distribution
0210014000 In distribution
0207070000 In distribution
0207054000 In distribution
0207065000 In distribution
0210008000S2 In distribution
0207060000 In distribution
0210018200 In distribution
0210010100S1 In distribution
0210007000 In distribution
0210008000 In distribution
0207057000 In distribution
0207067000 In distribution
0207052000 In distribution
0210010100 In distribution
0203030000 In distribution
0210018000 In distribution
0210100000S4 In distribution
0210003000 In distribution
0210015000 In distribution
0210004000 In distribution
0210004000s2 In distribution
0207059000 In distribution
0210034000 In distribution
0210012000 In distribution
0207055000 In distribution
0207068000 Withdrawn
0210016000 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
De Soutter Medical DE Soutter Medical Ltd. 65
InterPulse Stryker GmbH 41
Pulsavac® Zimmer Orthopaedic Surgical Products 35
MicroAire® Microaire Surgical Instruments LLC 34
Cleanest Guangzhou Clean Medical Products Manufacturing Corp 32
Simpulse Davol Inc. 31
AWI Apex (Suzhou) Medical Products Company 27
CarboJet® CO2 Bone Lavage System Kinamed, Inc. 26
Zksk Beijing Zksk Technology Co., Ltd. 20
Erbe Erbe Elektromedizin GmbH 18
AWI Apex (Guangzhou) Tools & Orthopedics Company 18
debritom+ Medaxis AG 17

Showing 12 of 98. All products under Lavage, Jet

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K873466 1987-11-06

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. 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
2017-11-09 Class II Environmental control Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates. 5988 2019-04-16
2015-05-08 Class II Package design/selection Potential sterility breach in the packaging. 5,328 each (444 boxes) 2015-10-19
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 330 2011-06-06
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 490 2011-06-06
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 103 2011-06-06
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 470 2011-06-06
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 490 2011-06-06
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 954 2011-06-06
2010-10-04 Not classified Packaging process control There is potential for a breach in sterility in the blister packaging. This can lead to the use of non-sterile product which, if contaminated, could lead to a patient infection. 350 2011-06-06

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