WoundExpress
FDA 510(k) K211200 · Huntleigh Healthcare , Ltd.
510(k) numberK211200
Submission
- Device name
- WoundExpress
- Applicant
- Huntleigh Healthcare , Ltd.
Cardiff, GB - Received
- April 22, 2021
- Decision date
- September 3, 2021
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JOW – Sleeve, Limb, Compressible
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5800
- Specialty
- Cardiovascular
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|---|---|---|---|
| K261807 | Sequential Circulator (SC-4004-DL, SC-4008-DL)JOW · Traditional | Bio Compression Systems, Inc. | 09/11/2026SE |
| K254217 | AerloomJOW · Traditional | Evolym, LLC | 08/31/2026SE |
| K253555 | Flexitouch® Plus Advanced Pneumatic Compression SystemJOW · Traditional | Tactile Medical | 07/31/2026SE |
| K253386 | DVT GarmentJOW · Traditional | Vistar Medical Supplies Co., Ltd. | 06/25/2026SE |
| K250242 | Compression Therapy Device (LGT-2202DVT)JOW · Traditional | Guangzhou Longest Medical Technology Co., Ltd. | 04/24/2026SE |
| K254267 | NanoPress 760A-BT (760A-BT)JOW · Traditional | Mego Afek , Ltd. | 02/24/2026SE |
| K250974 | Bio Arterial Deluxe (IC-BAP-DX)JOW · Traditional | Bio Compression Systems, Inc. | 12/12/2025SE |
| K250190 | Sequential Compression System (SCD600)JOW · Traditional | Shenzhen Comen Medical Instruments Co.,Ltd | 12/08/2025SE |
| K251466 | VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System…JOW · Special | Wellell, Inc. | 10/28/2025SE |
| K251446 | PlasmaFlow X Compression Sleeve Device (XPF0001)JOW · Special | Manamed, LLC | 09/17/2025SE |
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| K200975 | Sonicaid Team3 Antepartum, Sonicaid Team3 IntrapartumHGM · Traditional | 06/24/2020SE |
| K183574 | SRX Handheld Doppler, DMX Handheld Doppler, Obstetric Probes, Vascular ProbesDPW · Abbreviated | 09/06/2019SE |
| K152228 | Hydroven 12, Hydroven 12 GarmentsJOW · Traditional | 04/04/2016SE |
| K132650 | Sonicaid Freedom Wireless Fetal Monitoring SystemHGM · Traditional | 02/07/2014SE |
| K121108 | Dopplex AbilityJOM · Traditional | 01/03/2013SE |
| K090285 | Sonicaid FM820 and FM830 EncoreHGM · Traditional | 07/15/2009SE |
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Questions and answers
When was WoundExpress cleared by the FDA?
WoundExpress (K211200) received a 510(k) decision of Substantially Equivalent on September 3, 2021, 134 days after the submission was received.
What is the product code of K211200?
The FDA product code is JOW – Sleeve, Limb, Compressible, a Class II (moderate risk) device regulated under 21 CFR 870.5800.