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Spiggle & Theis Medizintechnik GmbH

US

Last updated September 17, 2026

Part of SPIGGLE & THEIS Medizintechnik GmbH

What Spiggle & Theis Medizintechnik GmbH makes

Spiggle & Theis Medizintechnik GmbH manufactures reusable surgical instruments for soft-tissue manipulation, including alligator forceps, irrigation/aspiration cannulas, and retraction tools. Their portfolio also includes specialized ENT devices such as nasal scissors, suction dissectors, and ear speculums, alongside precision instruments like micro forceps and suture hooks. Additional products include reusable curettes for endaural procedures and reusable tubular forceps for controlled tissue handling.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their instruments are designed for reusable medical use in surgical and otolaryngology applications, adhering to regulatory standards for reusable surgical tools 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 does Spiggle & Theis Medizintechnik GmbH manufacture?

Spiggle & Theis Medizintechnik GmbH manufactures reusable surgical instruments for soft-tissue manipulation, including alligator forceps, irrigation/aspiration cannulas, and retraction tools. They also produce specialized ENT devices such as nasal scissors, suction dissectors, and ear speculums, alongside precision instruments like micro forceps and suture hooks.

Where is Spiggle & Theis Medizintechnik GmbH based?

Spiggle & Theis Medizintechnik GmbH is based in the United States, as indicated by the country designation 'US' in the provided device data.

Which regulatory registries list Spiggle & Theis Medizintechnik GmbH's devices?

Spiggle & Theis Medizintechnik GmbH's devices are listed in the FDA's Unique Device Identifier (UDI) database, as specified in the device data.

How are Spiggle & Theis Medizintechnik GmbH's devices classified?

Spiggle & Theis Medizintechnik GmbH's devices are classified under FDA's Class I and Class II categories, as indicated in the device data. These classifications reflect the level of control necessary to ensure the safety and effectiveness of the devices.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+492206908165
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
332893028

Catalogue (2840)

Page 1 of 57
DeviceModel / ReferenceRegistriesClassStatus
Sterile equipment drape 2700061
FDA UDI
Class IIActive
Micro forceps, balanced, with plateau 40-836-15
FDA UDI
Class IActive
Grünwald tubular forceps 30-371-30
FDA UDI
Class IActive
Sickle knife 30-200-01
FDA UDI
Class IActive
Fraenkel tip 40-581-00
FDA UDI
Class IActive
Williger retractor 10-467-13
FDA UDI
Class IActive
Blakesley nasal forceps 20-215-03
FDA UDI
Class IActive
Suction dissector 30-1876
FDA UDI
Class IActive
Blakesley nasal forceps 30-350-03
FDA UDI
Class IActive
Suture hook 40-369-21
FDA UDI
Class IActive
Suction tube 10-300-15
FDA UDI
Class IActive
Micro ear forceps 10-703-06 TAN
FDA UDI
Class IActive
Sterile C-Arm / mobile x-ray cover 2900602
FDA UDI
Class IIActive
Fisch reference caliper 10-659-04
FDA UDI
Class IActive
Reference instrument 10-654-40
FDA UDI
Class IActive
Wullstein micro hook 10-630-04
FDA UDI
Class IActive
Shapleigh ear loop 10-266-02
FDA UDI
Class IActive
Selfholding Spekulum 30-711-00
FDA UDI
Class IActive
Stevens vessel scissors 20-625-11
FDA UDI
Class IActive
Fisch footplate elevator 10-643-02
FDA UDI
Class IActive
Ferguson suction tube 30-081-06
FDA UDI
Class IActive
Suction tube with interruptor, tip 50-349-30
FDA UDI
Class IActive
Micro scissors 20-793-15
FDA UDI
Class IActive
DeBakey needle holder 40-481-20
FDA UDI
Class IActive
Good-Scheckendiek tonsil scissors 40-430-19
FDA UDI
Class IActive
Farrior ear speculum 10-186-04
FDA UDI
Class IActive
House curette, double ended 10-667-03
FDA UDI
Class IActive
Trachea hook 80-340-04
FDA UDI
Class IActive
Davis-Boyle tongue depressor 40-313-05
FDA UDI
Class IActive
Hartmann ear forceps 10-276-00
FDA UDI
Class IActive
Miller nasal rasp, TC 20-806-01
FDA UDI
Class IActive
Spoon curette, semi-sharp 90-201-14
FDA UDI
Class IActive
ENT-single-use suction tubes, angled 303004
FDA UDI
Class IIActive
Bipolar connecting cable 80-320-30
FDA UDI
Class IIActive
Cottle osteotome 20-408-07
FDA UDI
Class IActive
Ballenger swivel knife 20-853-04
FDA UDI
Class IActive
Laryngeal mirror, rhodium coated 40-524-09
FDA UDI
Class IActive
Cottle chisel 20-409-04
FDA UDI
Class IActive
Fibreglass light carrier for laser 50-217-36
FDA UDI
Class IActive
Zöllner ear speculum 10-192-04
FDA UDI
Class IActive
Schuknecht micro hook 10-638-08
FDA UDI
Class IActive
Aufricht nasal retractor 20-568-16
FDA UDI
Class IActive
Bipolar connecting cable 80-324-40
FDA UDI
Class IIActive
Rochester-Pean artery forceps 40-650-33
FDA UDI
Class IActive
Joseph skin hook 20-895-15
FDA UDI
Class IActive
Farrior ear speculum 10-188-04
FDA UDI
Class IActive
Struempel ear forceps, straight 10-281-00
FDA UDI
Class IActive
Hook 50-317-23
FDA UDI
Class IActive
Wullstein micro needle 10-625-13
FDA UDI
Class IActive
Cottle-Walsham septum straightening 20-288-23
FDA UDI
Class IActive

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