AccuTec, Inc.

FDA Device Registration & Listing · VERONA, VA, US · Registration 1119522

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
1119522
FEI Number
1119522
Entity Name
AccuTec, Inc.
City/State/Country
VERONA, VA, US
Establishment Address
1 Razor Blade Ln, VERONA, VA 24482, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
AccuTec, Inc. (Owner Number: 10050196)
Owner / Operator Contact Address
1 Razor Blade Lane, Verona, VA 24482, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

General Surgery Tray Manual Instruments DermaBlade Skinceuticals DermaPlane DebrideBlade Microtome, Accessories Punch, Biopsy, Surgical

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRO General Surgery Tray General, Plastic Surgery Class 2 878.4370 2023-01-04
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2024-02-26
IDL Microtome, Accessories Pathology Class 1 864.3010 2015-10-20
EME Punch, Biopsy, Surgical Dental Class 1 872.4565 2019-07-31

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AccuTec, 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
K961683 J.J. Skinner, Inc. JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAY 1996-05-10

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2025 Windstone Medical Packaging, Inc. 2
Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0028-2025 Windstone Medical Packaging, Inc. 2
Aligned Medical Tonsil ENT Pack REF AMS9977 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0030-2025 Windstone Medical Packaging, Inc. 2
Aligned Medical T and A Pack REF AMS11482 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0031-2025 Windstone Medical Packaging, Inc. 2
Aligned Medical Tonsil Pack REF AMS14809 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0095-2021 Alcon Research, LLC 2
Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product Usage: used by ophthalmic surgeons in a variety of ophthalmic surgeries.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1119522. Last updated year: 2026. Please use registration number 1119522 when referencing this establishment in official correspondence.
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