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LANDANGER

US

Last updated May 23, 2026

What LANDANGER makes

The company manufactures reusable surgical instruments, including general-purpose scissors, soft-tissue manipulation forceps (both tweezers-like and scissors-like designs), suturing needle holders, retraction systems, retractor blades, and self-retaining retractors. Their portfolio also includes reusable instrument trays designed for surgical procedures.

All devices fall under Class I regulatory classification and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Landanger manufacture?

Landanger specializes in reusable surgical instruments. Their product range includes general-purpose surgical scissors, soft-tissue manipulation forceps (both tweezers-like and scissors-like), suturing needle holders, retraction systems, retractor blades, self-retaining retractors, and reusable instrument trays. These instruments are designed for use in surgical procedures.

Where is Landanger based?

Landanger is based in the United States. The company’s headquarters and manufacturing operations are located within the country.

Which regulatory registries list Landanger’s devices?

Landanger’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for Class I surgical instruments.

How are Landanger’s devices classified under medical device regulations?

All of Landanger’s devices fall under Class I regulatory classification. This classification applies to low-risk surgical instruments like reusable scissors, forceps, retractors, and trays, which are typically exempt from strict pre-market approval but still require compliance with FDA registration and UDI requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
299889175

Catalogue (3018)

Page 61 of 61
DeviceModel / ReferenceRegistriesClassStatus
Landanger B805251
FDA UDI
Class IActive
Delacroix-Chevalier DC20061-18
FDA UDI
Class IActive
Landanger B350090
FDA UDI
Class IActive
Landanger B259651
FDA UDI
Class IActive
Delacroix-Chevalier DC83221-44
FDA UDI
Class IActive
Landanger J00008
FDA UDI
Class IActive
Landanger B504598
FDA UDI
Class IActive
Delacroix-Chevalier DC21320-18
FDA UDI
Class IActive
Landanger B35190
FDA UDI
Class IActive
Landanger B40610
FDA UDI
Class IActive
Landanger B40132
FDA UDI
Class IActive
Delacroix-Chevalier DC20010-18
FDA UDI
Class IActive
Landanger B40210
FDA UDI
Class IActive
Delacroix-Chevalier DC20160-20
FDA UDI
Class IActive
Delacroix-Chevalier DC80013-30
FDA UDI
Class IActive
Landanger B400952
FDA UDI
Class IActive
Landanger B25486L
FDA UDI
Class IActive
Landanger B40071
FDA UDI
Class IActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Landanger CHAUMONT Haute-Marne · FR FEI 3005182241