Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Pilling Weck Group with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 11, 1997: PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCAR.
| Jun 11, 1997 | PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCARK971334 · GCJ | 510(k) clearances |
| Mar 4, 1997 | PILLING WECK 2 PIECE TAKE-APART INSTRUMENTSK965176 · OCZ | 510(k) clearances |
| Jan 10, 1997 | SECONDARY TROCAR AND SLEEVE WITH INSUFFLATION PORTK964450 · HET | 510(k) clearances |
| Dec 12, 1996 | REUSABLE TROCAR WITH SLEEVE (COMMON)K964123 · GCJ | 510(k) clearances |
| Nov 5, 1996 | REUSABLE TROCAR WITH SLEEVE (COMMON)K963815 · GCJ | 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
