Home › HU-FRIEDY MFG. CO., LLC › HU-FRIEDY
HU-FRIEDY
HU-FRIEDY MFG. CO., LLC · Model PKT3R · UDI-DI 10889950019082
5
510(k) clearances
10
Adverse events
1
Recalls
205
Facilities
Description
#3R Round Cone P.K. Thomas Waxing Inst.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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.
