VAN SICKLE SURGICAL INSTRUMENTS, INC.

FDA Device Registration & Listing · Hurst, TX, US · Registration 3034688516

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
3034688516
FEI Number
3034688516
Entity Name
VAN SICKLE SURGICAL INSTRUMENTS, INC.
City/State/Country
Hurst, TX, US
Establishment Address
116 W Harwood Rd Ste B, Hurst, TX 76054, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Van Sickle Surgical Instruments, Inc. (Owner Number: 10092324)
Owner / Operator Contact Address
116-B West Harwood Road, Hurst, TX 76054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle Van Sickle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDG Hook, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2024-12-23
HRR Scissors, Orthopedic, Surgical Orthopedic Class 1 888.4540 2025-08-21
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2025-08-21
FZT Cutter, Surgical General, Plastic Surgery Class 1 878.4800 2025-08-21
FTY Tape, Measuring, Rulers And Calipers General, Plastic Surgery Class 1 878.4800 2025-08-21
KBD Scissors, Nasal Ear, Nose, Throat Class 1 874.4420 2025-08-21
GEN Forceps, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2024-12-23
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2025-08-21
HRQ Hemostat General, Plastic Surgery Class 1 878.4800 2025-08-21
NNR Block, Cutting, Ent, Non-Sterile Ear, Nose, Throat Class 1 874.3540 2026-05-29
GAC Rasp, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2024-12-23
KBC Saw, Nasal Ear, Nose, Throat Class 1 874.4420 2026-05-29
KAD Elevator, Ent Ear, Nose, Throat Class 1 874.4420 2025-08-21
GAD Retractor General, Plastic Surgery Class 1 878.4800 2025-08-21
HOE Caliper, Ophthalmic Ophthalmic Class 1 886.4350 2025-08-21
HTD Forceps General, Plastic Surgery Class 1 878.4800 2025-08-21
KAS Knife, Nasal Ear, Nose, Throat Class 1 874.4420 2025-08-21
GDZ Handle, Scalpel General, Plastic Surgery Class 1 878.4800 2025-08-21
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2024-12-23
HXZ Cutter, Wire Orthopedic Class 1 888.4540 2026-05-29
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 2025-08-21

Official Correspondent

Mark Van Sickle

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Van Sickle Surgical Instruments, 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
K851170 The Huxley Instrument Corp. DISSECTING TWEEZER #283-72PCS. SS 410 1985-04-25
K821248 Conphar, Inc. ROCHESTER PEAN FORCEPS 1982-05-28
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09
K922626 Andronic Devices, Ltd. ADEPT INSTRUMENT POSITIONING ACCESSORY 1992-10-19
K820290 The Anspach Effort, Inc. SELF RETAINING RETRACTOR FOR HAND SURG 1982-03-05

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2014 Aesculap, Inc. 1
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
Z-0039-2018 Teleflex Medical 1
Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034688516. Last updated year: 2026. Please use registration number 3034688516 when referencing this establishment in official correspondence.
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