Foot Stool 10550
Foot Stool 10550 is a footstool (FDA Class I; FDA product code IKX, Aid, Transfer) made by Dynarex Corp., listed in FDA GUDID since 9 May 2022 (UDI-DI 00616784055015), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00616784055015 | Date9 May 2022 | StatusListed |
Official records
- AccessGUDID record 00616784055015
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Foot Stool
- Generic name
- Footstool
- Model / reference
- 10550
- Primary DI / UDI-DI
- 00616784055015
- FDA product code
- IKX
- GMDN term
- Footstool
- Device class
- Class I
- Regulation number
- 890.5050
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code IKX (Aid, Transfer).
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