Diamatrix Ltd.
Diamatrix · Model M23 · UDI-DI 00813059019691
HMR
Prescription
5
510(k) clearances
21
Adverse events
6
Recalls
96
Facilities
Description
Bores Axis Marker, Dual 4.5mm marking blades, Will work with any 12mm Mendez Degree Gauge, Diamond knurled handle, Stainless
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-23 | Aspen Surgical Products, Inc. | Fragments from the pad may disengage and stick to the instrument. The condition could cause fragments to come into contact with the intact cornea prior to surgery. |
| 2010-12-23 | Aspen Surgical Products, Inc. | Fragments from the pad may disengage and stick to the instrument. The condition could cause fragments to come into contact with the intact cornea prior to surgery. |
| 2010-12-23 | Aspen Surgical Products, Inc. | Fragments from the pad may disengage and stick to the instrument. The condition could cause fragments to come into contact with the intact cornea prior to surgery. |
| 2010-12-23 | Aspen Surgical Products, Inc. | Fragments from the pad may disengage and stick to the instrument. The condition could cause fragments to come into contact with the intact cornea prior to surgery. |
| 2010-12-23 | Aspen Surgical Products, Inc. | Fragments from the pad may disengage and stick to the instrument. The condition could cause fragments to come into contact with the intact cornea prior to surgery. |
| 2010-12-23 | Aspen Surgical Products, Inc. | Fragments from the pad may disengage and stick to the instrument. The condition could cause fragments to come into contact with the intact cornea prior to surgery. |
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.