Pharmaceutical companyLabelled 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 14, 2026, FDA's public records list Greer Laboratories, Inc. with 2 510(k) clearances and 2 device recalls. The most recent is a device recall dated Oct 25, 2022: GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY P….
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.
| Oct 25, 2022 | GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonsClass II · The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to | Device recalls |
| Oct 25, 2022 | GREER DIA - KIT ANTIGEN M. FAENI, 2.0mL 20 MG/ML, Analyte Specific Reagent, Item: K62, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusiClass II · The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to | Device recalls |
| Dec 13, 2000 | GREERTRACK SKIN TESTING SYSTEM, MODEL GT-IT, GT-ICK003195 · SCL | 510(k) clearances |
| Jun 23, 1989 | GREER DERMAPIK SYSTEMK890360 · SCL | 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
