Medical device makerLabelled 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 13, 2026, FDA's public records list Perlink USA, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 11, 1993: STERLING POWDER FREE PATIENT EXAMINATION GLOVES.
| Jun 11, 1993 | STERLING POWDER FREE PATIENT EXAMINATION GLOVESK922358 · LYY | 510(k) clearances |
| Mar 3, 1993 | STERLING LATEX EXAM GLOVE, HYPO-ALLERGENICK924959 · LYY | 510(k) clearances |
| Jun 23, 1992 | DISPOSABLE LATEX EXAMINATION GLOVESK921438 · LYY | 510(k) clearances |
| Aug 30, 1990 | PERLINK SCREEN, KIRAN SCREENK896707 · EAM | 510(k) clearances |
| Jul 11, 1990 | THERMOMETER, MERCURY/CLINICALK901790 · FLK | 510(k) clearances |
| May 7, 1990 | PERLINK CASSETTE, KIRAN CASSETTEK896708 · IXA | 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
