TANGIBLE SCIENCE Inc

FDA Device Registration & Listing · Campbell, CA, US · Registration 3012862899

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
3012862899
FEI Number
3012862899
Entity Name
TANGIBLE SCIENCE Inc
City/State/Country
Campbell, CA, US
Establishment Address
1055 Florence Way, Campbell, CA 95008, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Tangible Science (Owner Number: 10056543)
Owner / Operator Contact Address
1055 Florence Way, Campbell, CA 95008, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Tangible Hydrogel with Tangible Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens Etafilcon with Tangible™ Coating (etafilcon A) Soft (Hydrophilic) Daily Wear Contact Lens Tangible Boost

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2017-12-20
MVN Lens, Contact, (Disposable) Ophthalmic Class 2 886.5925 2017-12-20
MVN Lens, Contact, (Disposable) Ophthalmic Class 2 886.5925 2017-12-20
LPL Lenses, Soft Contact, Daily Wear Ophthalmic Class 2 886.5925 2017-12-20
QMM Hydrophilic Re-Coating Solution Ophthalmic Class 2 886.5919 2020-10-23

Official Correspondent

Katharine Kline

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tangible Science
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
K133079 Alden Optical Labs., Inc. IO2 SPHER(MANGOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IO2 TORIC (MANGOFILCON A) SOFT (HYDROPHILIC) 2013-12-17
K941998 Ocu-Ease Optical Products, Inc. OCU-FLEX-38 (POLYMACON) 1994-10-13
K992500 Cantor & Silver , Ltd. CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS 1999-08-18
K984098 Adventures IN Color Technology, Ltd. ADVENTURE TINTS, COLOR ENHANCED TINTED SOFT CONTACT LENS 1999-05-10
K003161 Les Laboratoires Blanchard ESSTECH MULTI TORIC ASPHERIC (MULTIFOCAL) (HIOXIFILCON B) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR (CLEAR AND TINT 2000-12-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0018-07 Ciba Vision Corporation 2
CSI Daily Wear, soft (hydrophilic) contact lenses
Z-0019-07 Ciba Vision Corporation 2
CSI Flexible Wear, soft (hydrophilic) contact lenses
Z-0020-07 Ciba Vision Corporation 2
CSI Toric, soft (hydrophilic) contact lenses
Z-0044-2012 CooperVision Inc. 2
AVAIRA Toric (enfilcon A) TORIC soft (Hydrophilic) Contact Lenses, 6 SOFT CONTACT LENSES FOR ASTIGMATISM, CooperVision, Scottsville, NY 14546 USA; Juana Diaz, PR 00795 USA; Hamble SO31, 4RF, UK; Device Listing # D033736. Product Usage: Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) in aphakic and non-aphakic persons with non-diseased eyes in powers from -20.00- to +20.00 diopters and astigmatic corrections from -0.25 to -10.00 diopters. The AVAIRA Soft Contact Lens is indicated for single - use disposable wear and daily wear. When prescribed for frequent replacement, the lens may be disinfected using a chemical or hydrogen peroxide disinfecting system.
Z-0326-2026 Alcon Research LLC 2
Alcon PRECISION1 One-Day Contact Lenses, -2.25D.

Similar Registrations

Registration Number Establishment Name Location
3013785060 CAMDEN PASSAGE Collingwood Ontario, CA
3008585940 GEO MEDICAL CO., LTD Buk-gu Gwangju, KR
3005994941 SOLOTICA INDUSTRIA E COMERCIO LTDA Sao Paulo, BR
3012590738 EYEYON MEDICAL Nes Ziona Central, IL
3025414414 SHENZHEN DASHICHENG OPTICAL TECHNOLOGY CO., LTD. Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012862899. Last updated year: 2026. Please use registration number 3012862899 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.