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Allergan

US

Last updated May 23, 2026

What Allergan makes

The company manufactures silicone gel-filled and saline-filled breast implants with smooth surfaces, including cohesive and unstructured designs. It also produces invasive breast implant sizers in fixed, reusable and single-use versions, as well as skin-port tissue expanders and tissue expander injection ports. Additionally, it supplies dermal tissue reconstructive materials derived from microbes, with and without anaesthetic properties.

These devices are classified under FDA categories Class II, Class III, and Unclassified (U) and are listed in the FDA’s Unique Device Identifier (UDI) database. 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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LinkedIn
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Email
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EUDAMED SRN
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Catalogue (1743)

Page 35 of 35
DeviceModel / ReferenceRegistriesClassStatus
Complete Brand Lubricating And Rewetting Drops K003109
FDA 510(k)
Class IIActive
Natrelle 133S Tissue Expander K182054
FDA 510(k)
UActive
Paco-Folder (tm) Intraocular Lens Forceps K864003
FDA 510(k)
Class IActive
Complete Brand Multi-Purpose Solution K980775
FDA 510(k)
Class IIActive
Mojave Cataract Extraction System K003638
FDA 510(k)
Class IIActive
Complete Brand Multi-Purpose Solution K014202
FDA 510(k)
Class IIActive
Ultracare Neutralizing Tablets K984383
FDA 510(k)
Class IIActive
Refresh Contacts Lubricating And Rewetting Drops K992028
FDA 510(k)
Class IIActive
Single Amplifier For Botox K051852
FDA 510(k)
Class IIActive
New Use For Acuvac Suction Reservoir 400cc K863201
FDA 510(k)
Class IActive
Soakare K821052
FDA 510(k)
UActive
Complete Brand Comfortplus Multi-Purpose Solution K000164
FDA 510(k)
Class IIActive
TrueTear Intranasal Tear Neurostimulator DEN170086
FDA 510(k)
Class IIActive
Clean-N-Soak K822707
FDA 510(k)
UActive
TrueTear Intranasal Tear Neurostimulator K193589
FDA 510(k)
Class IIActive
Amo Prestige Day Pack (allergan, Inc.) K962402
FDA 510(k)
Class IIActive
Lenskeeper Contact Lens Carrying Case K861642
FDA 510(k)
UActive
Natrelle 133 Plus MICROCELL Tissue Expander K180826
FDA 510(k)
UActive
Refresh Optive Lens Comfort Rewetting Drops K083812
FDA 510(k)
Class IIActive
Liquifilm Wetting Solution K821051
FDA 510(k)
UActive
REFRESH RELIEVA For CONTACTS K190674
FDA 510(k)
Class IIActive
Bks-42 Disposable Vacuum Tubing Pack K864065
FDA 510(k)
Class IActive
Blink-N-Clean K821055
FDA 510(k)
UActive
Complete Brand Lubricating And Rewetting Drops K983150
FDA 510(k)
Class IIActive
Amo Diplomax/Opsys Console K971186
FDA 510(k)
Class IIActive
Seri Surgical Scaffold K123128
FDA 510(k)
Class IIActive
Natrelle 133 Plus Tissue Expander K143354
FDA 510(k)
UActive
Pre-Sert K822706
FDA 510(k)
UActive
Bks-1000 Refractive Set Use In Keratorefractive K870807
FDA 510(k)
Class IActive
Complete Brand Multi-Purpose Solution K003252
FDA 510(k)
Class IIActive
NATRELLE INSPIRA Single Use Sizers for Gel Implants K203229
FDA 510(k)
UActive
Amo Phacoflex Ii Intersection System K961242
FDA 510(k)
Class IActive
Sovereign Cataract Extraction System K981116
FDA 510(k)
Class IActive
Total K821054
FDA 510(k)
UActive
Complete Brand Multi-Purpose Solution, Complete Brand Lubricating And Rewetting Drops K981168
FDA 510(k)
Class IIActive
Angel Chik Anti-Reflux Prosthesis P790006
FDA PMA
Class IIIActive
NATRELLE Highly Cohesive Anatomically Shaped Silicone-Filled P040046
FDA PMA
Class IIIActive
Juvéderm® Voluma® XC P110033
FDA PMA
Class IIIActive
Natrelle Saline-Filled Breast Implants P990074
FDA PMAFDA UDI
Class IIIActive
Natrelle Silicone-Filled Breast Implants P020056
FDA PMA
Class IIIActive
Contigen Bard Collagen Implant P900030
FDA PMA
Class IIIActive
Zyderm Collagen Implant (zyderm Ci) P800022
FDA PMA
Class IIIActive
Juvéderm Hyaluronate Gel Implants P050047
FDA PMA
Class IIIActive

Related Companies

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FDA Establishments (2)

Establishments registered with the FDA under this company group, matched by name.

  • Allergan LA AURORA DE HEREDIA · CR FEI 3006108784
  • Allergan Annecy Haute-Savoie · FR FEI 3005113652