AURORA SURGICAL, LLC

FDA Device Registration & Listing · St Petersburg, FL, US · Registration 3009027787

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
3009027787
FEI Number
3009027787
Entity Name
AURORA SURGICAL, LLC
City/State/Country
St Petersburg, FL, US
Establishment Address
780 94th Avenue N, Suite 108, St Petersburg, FL 33702, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device
Owner / Operator
Aurora Surgical, LLC (Owner Number: 10037164)
Owner / Operator Contact Address
780 94th Ave N, Suite 108, St Petersburg, FL 33702, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Schocket Double Ended Scleral Depressor Identification Marking Tape Roll Instrument Marking Tape Kelly Punch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2011-06-22
FHQ Holder, Needle, Gastroenterologic Gastroenterology, Urology Class 1 876.4730 2011-06-22
HNF Scissors, Ophthalmic Ophthalmic Class 1 886.4350 2011-06-22
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 2011-06-22
HNX Depressor, Orbital Ophthalmic Class 1 886.4350 2023-12-07
HOB Clamp, Muscle, Ophthalmic Ophthalmic Class 1 886.4350 2011-06-22
HKW Prism, Bar, Ophthalmic Ophthalmic Class 1 886.1650 2011-06-22
HOD Clamp, Eyelid, Ophthalmic Ophthalmic Class 1 886.4350 2011-06-22
MXY Cannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl Acetal Ophthalmic Class 1 886.4350 2011-06-22
HRP Pen, Marking, Surgical Ophthalmic Class 1 886.4570 2019-05-30
HNQ Hook, Ophthalmic Ophthalmic Class 1 886.4350 2011-06-22
LYV Label Or Tag, Sterile General, Plastic Surgery Class 1 878.4800 2023-12-07
HOH Spectacle, Operating (Loupe), Ophthalmic Ophthalmic Class 1 886.4770 2011-06-22
GEN Forceps, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2011-06-22
HNJ Punch, Corneo-Scleral Ophthalmic Class 1 886.4350 2023-12-07
GAF Spatula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2011-06-22
HNZ Curette, Ophthalmic Ophthalmic Class 1 886.4350 2011-06-22
GFF Bur, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4820 2011-06-22
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2011-06-22
GEG Elevator, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2011-06-22

Official Correspondent

Lena Jonsson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aurora Surgical, LLC
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
K851170 The Huxley Instrument Corp. DISSECTING TWEEZER #283-72PCS. SS 410 1985-04-25
K821248 Conphar, Inc. ROCHESTER PEAN FORCEPS 1982-05-28
K871646 Ocular Instruments, Inc. TANNE CORNEAL CUTTING BLOCK 1987-05-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009027787. Last updated year: 2026. Please use registration number 3009027787 when referencing this establishment in official correspondence.
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