Kelly Grasping Forceps 2901-214

GUDID 00192896120167

Kelly Grasping Forceps Double Action Jaws

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable

• Primary Device ID: 00192896120167
• NIH Device Record Key: 26abc27f-200a-4cae-9de5-407bf2779fdf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kelly Grasping Forceps
• Version Model Number: 2901-214
• Catalog Number: 2901-214
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896120167 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102921

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

[00192896120167]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-23
• Device Publish Date: 2024-10-15

Devices Manufactured by SONTEC INSTRUMENTS, INC.

• 00192896105171 - Small Plates: 2026-03-27 Small Plates For Use With Bending Pliers
• 00192896122833 - Intraocular Set: 2026-03-27 Intraocular Set - 2 Forceps 2 Scissors With Tray
• 00192896122840 - Alyea-Babcock Vasectomy Clamp: 2026-03-27 Alyea-Babcock Vasectomy Clamp
• 00192896122857 - Diamond Head Grasping Forceps: 2026-03-27 Diamond Head Grasping Forceps With Flushing Port Straight 2.7 Millimeter
• 00192896122864 - Velociraptor Junior Rongeur: 2026-03-27 Velociraptor Junior Rongeur Straight Shaft 2.7 Millimeter Tip With Flushing Port
• 00192896122871 - Spoon Curette: 2026-03-27 Spoon Curette 45 Degree
• 00192896122888 - Dissector: 2026-03-27 Dissector Softly Curved
• 00192896122895 - Ball Dissector: 2026-03-27 Ball Dissector Softly Curved