Bone Conduction Hearing Aid (G41157, G41158, G41159, G41160, G42151, G42152, G42153, G42154, G42155, G42156, G42157, G42158, G42159, G42160, G43151, G43152, G43153, G43154, G43155, G43156, G45151, G45152, G45153, G45154, G45155, G45156, G45157, G45158, G45159, G45160, G46151, G46152, G46153, G46154, G46155, G46156, G46157, G46158)
K260452 is the FDA 510(k) clearance record for Bone Conduction Hearing Aid (G41157, G41158, G41159, G41160, G42151, G42152, G42153, G42154, G42155, G42156, G42157, G42158, G42159, G42160, G43151, G43152, G43153, G43154, G43155, G43156, G45151, G45152, G45153, G45154, G45155, G45156, G45157, G45158, G45159, G45160, G46151, G46152, G46153, G46154, G46155, G46156, G46157, G46158), a class II device, cleared for Zdeer Technology (Henan) Co., Ltd. on under FDA product code LXB (Hearing Aid, Bone Conduction). FDA records list 2 510(k) clearances for Zdeer Technology (Henan) Co., Ltd., from to . As of , FDA records show no recalls naming K260452.
Clearance record
- Decision date
- Received
- (124 days to decision)
- Product code
- LXB Hearing Aid, Bone Conduction
- Regulation
- 21 CFR 874.3302
- Device class
- Class II
- Review panel
- Ear, Nose, Throat
- Applicant
- Zdeer Technology (Henan) Co., Ltd. East Of Wei Wu Rd. And S. Of Qin Gong E. Rd.,, Changge, Xuchang City, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code LXB
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 2 |
| July 2026 | 1 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
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