Park Dental Research Corp

GUDID D769OKIT20

Deluxe Surgical Kit

PARK DENTAL RESEARCH CORP

Dental implant/prosthesis surgical procedure kit Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: D769OKIT20
• NIH Device Record Key: ad084e0e-ab74-4862-b560-e3b57b181830
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Park Dental Research Corp
• Version Model Number: OKIT-2
• Company DUNS: 011441508
• Company Name: PARK DENTAL RESEARCH CORP
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com
• Phone: 1-800-243-7372
• Email: info@pdrus.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D769OKIT20 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

[D769OKIT20]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-11-09

On-Brand Devices [Park Dental Research Corp]

• D769P90410: 4.2 mm Depth Gauge
• D769P90380: 3.75mm Depth Gauge
• D769P90330: 3.3 mm Depth Gauge
• D769RATC800: Continuous Feedback Torque Wrench 15-80 Ncm
• D769P33110: 3.3 mm x 11.5 mm StarVent Implant with cover screw and implant driver short
• D769P17500: 5.0mm Irrigated Drill (Outer Ø 4.5mm)
• D769OR125: O-Ring Large (25 pack)
• D769OKIT20: Deluxe Surgical Kit
• D769DRVRT2040: 3.0 Multi-Purpose Driver 2.04 mm / 2.0 mm O-Ball Abutment Driver Short
• D769DRT150: 1.5mm Surgical Drill
• D769ACAN30: 3.0mm Multi-Platform Analog
• D7692513XO0: 2.5 mm X 13 mm LEW Mini Implant Non-Collared