PRECISION OPHTHALMIC INSTRUMENT SERVICES, LLC.

FDA Device Registration & Listing · Brighton, MI, US · Registration 3037687712

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
3037687712
FEI Number
3037687712
Entity Name
PRECISION OPHTHALMIC INSTRUMENT SERVICES, LLC.
City/State/Country
Brighton, MI, US
Establishment Address
8732 River Valley Rd, Brighton, MI 48116, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Precision Ophthalmic Instrument Services, LLC. (Owner Number: 10093163)
Owner / Operator Contact Address
8732 River Valley Road, Brighton, MI 48116, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Precision LED AC900 Digital Acuity Chart Precision RT-100 Refractor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2025-04-09
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2025-04-09

Official Correspondent

Tamatha Barnes

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Precision Ophthalmic Instrument Services, LLC.
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 3037687712. Last updated year: 2026. Please use registration number 3037687712 when referencing this establishment in official correspondence.
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