Home › PREMIER DENTAL PRODUCTS COMPANY › 2PRO
2PRO
PREMIER DENTAL PRODUCTS COMPANY · Model 5500303 · UDI-DI 00348783004397
EHK
Prescription
8
510(k) clearances
3
Adverse events
1
Recalls
121
Facilities
Description
2PRO Angle Soft/Long White (144)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-07-20 | Cosmedent, Inc. | Reports were received the elastomer cup material is crumbling. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.