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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Apothecary Products, LLC with 6 510(k) clearances and 2 device recalls. The most recent is a device recall dated Mar 30, 2023: Eye and Ear Dropper, Product Code 67082.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 30, 2023 | Eye and Ear Dropper, Product Code 67082Class II · Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. | Device recalls |
| Mar 30, 2023 | Medicine Dropper, Product Code K508Class II · Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. | Device recalls |
| Jul 9, 2014 | FLENTS PLASTIC EYE WASH CUPK140409 · LXQ | 510(k) clearances |
| Jul 14, 2011 | SOFT GRIP CONTACT LENS CASE, DELUXE CONTACT LENS CASE, ECONO-MATE CONTACT LENS CASEK111856 · LRX | 510(k) clearances |
| Nov 26, 2004 | EZY-TRAVEL WRISTBANDK041766 · MVV | 510(k) clearances |
| Jun 25, 2002 | ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057K020296 · EWD | 510(k) clearances |
| May 12, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K892242 · LYY | 510(k) clearances |
| Feb 4, 1984 | NITROGLYCERINE CONTAINERK833311 · NXB | 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
