ALTAIRE PHARMACEUTICALS, INC.

FDA Device Registration & Listing · AQUEBOGUE, NY, US · Registration 2335740

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2335740
FEI Number
1000119582
Entity Name
ALTAIRE PHARMACEUTICALS, INC.
City/State/Country
AQUEBOGUE, NY, US
Establishment Address
311 WEST LN., AQUEBOGUE, NY 11931, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ALTAIRE PHARMACEUTICALS, INC. (Owner Number: 9047159)
Owner / Operator Contact Address
311 WEST LN., P O Box 849, Aquebogue, NY 11931, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Lobob Cleaner Lobob W/RW Drop Lobob C/D/S Solution Altaire MPS#1 Multipurpose Contact

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2007-11-26
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2007-11-26
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2007-11-26
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2007-11-26
MRC Products, Contact Lens Care, Rigid Gas Permeable Ophthalmic Class 2 886.5918 2007-11-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ALTAIRE PHARMACEUTICALS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K093254 Abbott Medical Optics, Inc. AMO BRAND MULTI-PURPOSE DISINFECTING SOLUTION 2010-09-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0028-05 Ciba Vision Corporation 2
SOLO-care Plus with Aqualube, Multi-purpose solution*** AquaSoft (Private label), Multi-purpose solution***Sterile***For soft lenses, CIBA Vision Corporation, Made in Canada, Assembled in Canada, Manufactured for: CIBA Vision Corporation, Duluth, GA 30097 USA. The product is distributed in units of single or twin packs containing 2 to 12 ounces of product.
Z-0129-2011 Abbott Medical Optics Inc (AMO) 2
AMO COMPLETE Multi-Purpose Solution, Formula: 9424x; Product Code: 93504 (360ml), 93505 (2x 360ml duo pack), 93515 (240 ml). Cleans, rinses, disinfects, and stores all soft contact lenses and helps keep your eyes protected from dryness and irritation throughout the day.
Z-0130-2011 Abbott Medical Optics Inc (AMO) 2
AMO Total Care (1) Contact Lens Solution, Formula: 8772x; Product Code: 90275 (240 ml). Relieves the dryness, irritation, and discomfort that may be associated with contact lens wear.
Z-0030-2022 Contamac Solutions, Inc. 2
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2335740. Last updated year: 2026. Please use registration number 2335740 when referencing this establishment in official correspondence.
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