Pharmaceutical companyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AbbVie. FDA records under 9 spellings of its name, each linked to the record. See the AbbVie group view.
As of Nov 13, 2026, FDA's public records list Allergan with 55 drug applications, 38 510(k) clearances, 24 device recalls, 9 drug recalls and 1 warning letter. The most recent is a 510(k) clearance dated Jun 2, 2021: NATRELLE INSPIRA Single Use Sizers for Gel Implants.
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.
| Date | Record | Source |
|---|---|---|
| Jun 2, 2021 | NATRELLE INSPIRA Single Use Sizers for Gel ImplantsK203229 · MRD | 510(k) clearances |
| Aug 31, 2020 | TrueTear Intranasal Tear NeurostimulatorK193589 · QBR | 510(k) clearances |
| Jul 6, 2020 | Skin Medica Acne System, Contains: Purifying Foaming Wash (Salicylic Acid 2.0%), 5 fl oz.; Purifying Toner (Salicylic Acid 2.0%), 6 fl oz,; Class III · SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints. | Drug recalls |
| Jul 6, 2020 | Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%), 2 Oz bottle, Distributed in the U.S.A. by Allergan, Irvine, CA 92612, NDC 0023-49Class III · SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints. | Drug recalls |
| May 14, 2020 | Warning letter: 510(k) requiredCDRH | Warning letters |
| Aug 8, 2019 | REFRESH RELIEVA For CONTACTSK190674 · LPN | 510(k) clearances |
| Dec 21, 2018 | Natrelle 133 Plus MICROCELL Tissue ExpanderK180826 · LCJ | 510(k) clearances |
| Aug 29, 2018 | Natrelle 133S Tissue ExpanderK182054 · LCJ | 510(k) clearances |
| May 17, 2018 | TrueTear Intranasal Tear NeurostimulatorDEN170086 · QBR | 510(k) clearances |
| Nov 21, 2016 | XEN Glaucoma Treatment SystemK161457 · KYF | 510(k) clearances |
| Aug 20, 2015 | Natrelle 133 Plus Tissue ExpanderK143354 · LCJ | 510(k) clearances |
| Jun 18, 2015 | Natrelle 133 Series Tissue Expanders Product Usage: Natrelle 133 Series Tissue Expander is intended for temporary subcutaneous implantatClass II · Allergan is recalling the NATRELLE 133 and CUI Series Tissue Expanders because the product shipped was beyond the 47 mon | Device recalls |
| Jun 18, 2015 | Natrelle CUI Series Tissue Expanders. Product Usage: Natrelle CUI Series Tissue Expander has been designed for temporary implantation toClass II · Allergan is recalling the NATRELLE 133 and CUI Series Tissue Expanders because the products shipped were beyond the shel | Device recalls |
| Jun 8, 2015 | Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc, Style No. MSZFX410. The product is packaged in a thermoformed tray (double sClass II · Allergan is recalling the NATRELLE 410cc Re-Sterilizable Breast Implant Sizer because the expired product was shipped to | Device recalls |
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
