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Sign in to claim this brandApothecary Products, Inc.
US
Last updated May 23, 2026
What Apothecary Products, Inc. makes
Apothecary Products, Inc. manufactures pill crushers and splitters for medication management, single-use earplugs for hearing protection, contact lens cases for hygiene, manual lice combs for head lice removal, finger-cot surgical drapes for procedural use, single-use public respirators for infection control, acupressure wristbands for self-care, and urine test strip colour charts as an in vitro diagnostic tool for urine analysis.
The company’s products are regulated under FDA classifications including Class I, Class II, and unclassified (U), with submissions recorded in the 510(k), PMA, and UDI registries. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
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Catalogue (149)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Acu-Life (HE) | 400881 | FDA UDI | Class I | Active |
| Flents Protechs | 70321 | FDA UDI | U | Active |
| Flents | 70129 | FDA UDI | Class II | Active |
| Flents | 68840/HK68840 | FDA UDI | U | Active |
| Flents | 68405 | FDA UDI | U | Active |
| Ezy Dose | 67755P | FDA UDI | Class I | Active |
| Cdc | F405-620CD | FDA UDI | Class II | Unknown |
| Flents | 70279 | FDA UDI | U | Active |
| Care One | F406-906CO1 | FDA UDI | U | Active |
| Ezy Dose | 70282 | FDA UDI | Class I | Active |
| Flents Protechs | 68055 | FDA UDI | U | Active |
| Ezy Dose | 68259GAMT | FDA UDI | Class I | Active |
| Acu-Life | PC12/HKPC12/PC12WE | FDA UDI | Class I | Active |
| Ezy Dose | 67825/67825AZ/HK67825 | FDA UDI | Class I | Active |
| Flents Protechs | 68054 | FDA UDI | U | Active |
| Ezy Dose | 67820 | FDA UDI | Class I | Active |
| Ezy Dose | 67755BL | FDA UDI | Class I | Active |
| Ezy Dose Kids | C265 | FDA UDI | U | Active |
| Flents | 68012 | FDA UDI | Class II | Active |
| Flents | 69626 | FDA UDI | Class I | Active |
| Ezy Dose | 67015BC1 | FDA UDI | Class I | Active |
| Ezy Dose | 67661/HK67661/67661NI | FDA UDI | Class I | Active |
| Acu-Life (HE) | 400711 | FDA UDI | U | Active |
| Flents | F408-145/F408-145AZ | FDA UDI | U | Active |
| Ezy Dose | MC12/MC12A | FDA UDI | Class I | Active |
| Cdc | C283CD1 | FDA UDI | Class II | Active |
| Flents Protechs | 68033 | FDA UDI | U | Active |
| Flents | 70121 | FDA UDI | U | Active |
| Flents | F408-155 | FDA UDI | U | Active |
| Flents | K1010 | FDA UDI | Class II | Active |
| Ezy Dose | 67755G | FDA UDI | Class I | Active |
| Ezy Dose | 68259PAMT | FDA UDI | Class I | Active |
| Ezy Dose | 68255BL | FDA UDI | Class I | Active |
| Acu-Life (HE) | 400531 | FDA UDI | Class I | Active |
| Rexall | 68076DG | FDA UDI | U | Active |
| Flents Protechs | 68052 | FDA UDI | U | Active |
| Core Values | 400830 | FDA UDI | Class I | Active |
| Rite Aid | K1010RA | FDA UDI | Class II | Active |
| Ezy Dose | 80199 | FDA UDI | Class I | Active |
| Ezy Dose | 67015BKAMT | FDA UDI | Class I | Active |
| Ezy Dose | 69315 | FDA UDI | Class I | Active |
| Acu-Life | 400711A | FDA UDI | U | Active |
| Patient Examination Gloves (latex) | K892242 | FDA 510(k) | Class I | Active |
| Flents Plastic Eye Wash Cup | K140409 | FDA 510(k) | U | Active |
| Nitroglycerine Container | K833311 | FDA 510(k) | Class I | Active |
| Ezy-Travel Wristband | K041766 | FDA 510(k) | U | Active |
| Adult Silicone Ear Plugs, Models # 68053, 68057 | K020296 | FDA 510(k) | U | Active |
| Soft Grip Contact Lens Case, Deluxe Contact Lens Case, Econo-Mate Contact Lens Case | K111856 | FDA 510(k) | Class II | Active |
| The Normaline Kit | P800055 | FDA PMA | Class II | Active |
Related Companies
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Apothecary Products, Inc. has two recall records, both initiated on March 30, 2023. One record is marked as open, while the other is classified. The reasons provided in both cases involve the potential presence of glass particulate on the outside surface of a glass dropper bulb.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 30, 2023 | Z-1703-2023 | — | open, classified | Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. |
| Mar 30, 2023 | Z-1702-2023 | — | open, classified | Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. |