Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Smith & NephewLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Smith & Nephew, Mpl Division with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 27, 1984: MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE.
| Sep 27, 1984 | MPL HYPO BRAND BREECH LOAD ASPIR SYRINGEK843314 · EJI | 510(k) clearances |
| May 21, 1984 | SOLOPAK BRAND FILTER NEEDLE W/5 MICROK841280 · FPB | 510(k) clearances |
| Apr 5, 1984 | MAX-I-PROBE PERIODONTAL ENDODONTIC PROBK840237 · EIC | 510(k) clearances |
| Mar 30, 1984 | HYPO BRAND DISPOS. DENTAL NEEDLES-PLASTK833304 · DZM | 510(k) clearances |
| Aug 12, 1983 | MICRO Z DISPOS. SPINAL ANESTH. NEEDLEK832126 · BSP | 510(k) clearances |
| Jul 12, 1983 | HERAPIN LOCK FLUSH SOLUTION USE KITK831765 · FMI | 510(k) clearances |
| Mar 24, 1983 | HENKE JECT PRESSURE SYRINGEK830524 · EJI | 510(k) clearances |
| Feb 15, 1983 | MICRO 2 HYPODERMIC NEEDLESK830242 · FMI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
