ReminGel
FDA 510(k) clearance K241489 · decided 2025-01-08
Clearance details
- K-number
- K241489
- Device name
- ReminGel
- Applicant
- Inter-Med, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2024-05-24
- Decision date
- 2025-01-08
- Days to decision
- 229 days
- Clearance type
- Traditional
- Product code
- LBH
- Device class
- 2
- Regulation number
- 872.3260
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Racine, WI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.