GUDIDData
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gudid Primary ID: LS2000

SUMMIT MEDICAL (UDI LS2000)

Manufactured by Summit Medical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SUMMIT MEDICAL - Primary ID LS2000

Device Regulatory Overview

The SUMMIT MEDICAL (Model/Catalog Number: LS2000) is a medical device manufactured by Summit Medical, Inc.. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1319-2013 View Full Alert →

Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit Medical, Inc., 815 Northwest Parkway, Suite 100, St. Paul, MN...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-0435-2016 View Full Alert →

AbsorbENT, Sterile Compressed Absorbent Sponge, Nasal Pack, 8.9cm(L) x 3.0cm (W) x 1.5cm (H), RH-7413-10, Sterilized by Gamma Radiation, Rx...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1731-2014 View Full Alert →

Armstrong Grommet with wire Otological Ventilation Tube Catalog #: VT-0507-01, Sterilized by Ethylene Oxide, Rx Only. Intended to provi...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
LS2000
Product Code / EMDN
KDQ
Device Name
Database Sync Date
2026-08-09 09:31:12

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of SUMMIT MEDICAL?

The registered manufacturer of record for SUMMIT MEDICAL is Summit Medical, Inc..

What is the Primary UDI-DI identifier for SUMMIT MEDICAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LS2000.

What classification code is assigned to this device?

This device is registered under product classification code KDQ.

Similar Classification Devices (KDQ)

Other Devices by Summit Medical, Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint