Data / Medical devices / Ingested, Transient, Space Occupying Device For Weight Management And/Or Weight Loss
Ingested, Transient, Space Occupying Device For Weight Management And/Or Weight Loss (QFQ): 4 FDA-registered makers in 4 countries
4 establishments in 4 countries are registered with the FDA to make Ingested, Transient, Space Occupying Device For Weight Management And/Or Weight Loss (product code QFQ, Class 2, 21 CFR 876.5982). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on October 2, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- QFQ
- Device class
- 2
- Regulation
- 876.5982
- Medical specialty
- Gastroenterology, Urology
Makers by country
| Country | Makers |
|---|---|
| Israel | 1 |
| Italy | 1 |
| Mexico | 1 |
| China | 1 |
Makers of Ingested, Transient, Space Occupying Device For Weight Management And/Or Weight Loss
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Epitomee Medical Ltd. | Caesarea Central, Israel | Manufacturer | 1 | September 13, 2024 | 0 | 0 | 0 | api.fda.gov |
| Gelesis SRL | Calimera Lecce, Italy | Manufacturer | 1 | January 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Centerpiece S. De R.L De C.V | Playas de Rosarito Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Bonliter Optoelectronic Co., Ltd. | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated October 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.