ADAPTIVE SENSORY TECHNOLOGY INC

FDA Device Registration & Listing · San Diego, CA, US · Registration 3013682704

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
3013682704
FEI Number
3013682704
Entity Name
ADAPTIVE SENSORY TECHNOLOGY INC
City/State/Country
San Diego, CA, US
Establishment Address
9823 Pacific Heights Blvd, Suite CD, San Diego, CA 92121, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Adaptive Sensory Technology Inc (Owner Number: 10054838)
Owner / Operator Contact Address
9823 Pacific Heights Blvd,Ste CD, San Diego, CA 92121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Manifold Contrast Vision Meter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2020-06-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Adaptive Sensory Technology Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013682704. Last updated year: 2026. Please use registration number 3013682704 when referencing this establishment in official correspondence.
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