Home › Heine Optotechnik GmbH & Co. KG › HEINE® FO Anoscopes with annular FO Illumination
HEINE® FO Anoscopes with annular FO Illumination
Heine Optotechnik GmbH & Co. KG · Model 000 · UDI-DI 04053755126705
10
510(k) clearances
86
Adverse events
1
Recalls
46
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-12-12 | Applied Medical Resources Corp | Unintentional shifting of the tip insulation of the firm's electrosurgical probes. |
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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.
