Plenity
FDA 510(k) clearance K230133 · decided 2024-01-19
Clearance details
- K-number
- K230133
- Device name
- Plenity
- Applicant
- Gelesis, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2023-01-17
- Decision date
- 2024-01-19
- Days to decision
- 367 days
- Clearance type
- Traditional
- Product code
- QFQ
- Device class
- 2
- Regulation number
- 876.5982
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Boston, MA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Epitomee (K240544) | Epitomee Medical , Ltd. | 2024-09-13 |
| Plenity (DEN180060) | Gelesis, Inc. | 2019-04-12 |
Recalls involving this device
No recalls on record reference this clearance.