WillowWood Global, LLC
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000050990
- Devices
- 3,301
- Registrations
- EUDAMEDFDA
- FDA recalls
- 11 ongoing
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA establishment, FDA recalls
Catalogue
Search and filter all 3,301 devicesShowing 1-50 of 3,301
Company details
- EUDAMED SRN
- US-MF-000050990
- DUNS number
- 004280723
- EUDAMED status
- Active
- EUDAMED registered name
- WillowWood Global, LLC
- EUDAMED abbreviated name
- WWG
- Registered address
- 15441, Scioto Darby Road, 43143, Mount Sterling, United States
- Website
- willowwood.com
- linkedin.com/company/508181
- facebook.com/willowwoodglobal
- [email protected]
- Phone
- tel:+7408693377
- PRRC contact
- Steve Huggins
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 1
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2021
- 20 Apr 2021 Z-1594-2021 Class II Ongoing the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was used in place of the 5/8 pin. Over time, the shorter pin may not engage in either the upper or lower body, causing the cord to come loose or slip which could result in the loss of suspension.
Full distribution text
- 20 Apr 2021 Z-1594-2021 Class II Ongoing the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was used in place of the 5/8 pin. Over time, the shorter pin may not engage in either the upper or lower body, causing the cord to come loose or slip which could result in the loss of suspension.
FDA establishments
- WillowWood Global LLC Mt Sterling, OH · US FEI 1522166
From the company website
Innovating for clinicians and patients has been the primary focus of WillowWood since the company was founded in Ohio in 1907. Partnered with Blue Sea Capital, our sole purpose is to be the industry leader enabling the best clinical outcomes for amputees.
Frequently asked questions
How many devices does WillowWood Global, LLC have in the registry?
The registry currently lists 3301 devices for WillowWood Global, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list WillowWood Global, LLC's devices?
Among its 50 most recently registered devices, WillowWood Global, LLC has devices listed in EUDAMED (50 devices).
What risk classes do WillowWood Global, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for WillowWood Global, LLC's devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for WillowWood Global, LLC?
FDA recall records list 1 recall initiated by WillowWood Global, LLC, the most recent initiated on 2021-04-20. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from WillowWood Global, LLC in the registry?
The most recently registered devices listed for WillowWood Global, LLC include SFP-31LB-4L, AKNYSERTS, 700-MGL492 and K001-28L-2.
Which FDA establishments are linked to WillowWood Global, LLC?
1 FDA establishment is linked to WillowWood Global, LLC in the registry; they are listed on the company page.