Lavage, Jet
Femoral Canal Brush, Irrigation/Suction with Increased Suction
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.
| 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
| 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
| 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 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
| 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
| 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.
| 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.