company
Beta Bionics, Inc.
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-24Beta Bionics, Inc. — Class II recall: iLet Bionic Pancreas, REF: BB1001
- fda_recall · device_recall2026-05-06Beta Bionics, Inc. — Class II recall: iLet Bionic Pancreas, REF: BB1001
- fda_recall · device_recall2026-04-22Beta Bionics, Inc. — Class II recall: iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
Frequently asked questions
- How many FDA warning letters has Beta Bionics, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Beta Bionics, Inc. in our current dataset.
- What FDA recalls has Beta Bionics, Inc. issued?
- Argus HQ has recorded 3 FDA recalls tied to Beta Bionics, Inc..
- Is Beta Bionics, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 3 recalls, and 0 approval records for Beta Bionics, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.