← Back to catalogue

Tebbetts Hand-Activated Monopolar Insulated Forcep

FDA UDI

Class II (US FDA UDI)

by Black & Black Surgical, Inc.

Identity

Trade Name
Tebbetts Hand-Activated Monopolar Insulated Forcep FDA UDI
Generic Name
Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
TEBBETTS ELECTROSURGICAL MONO-POLAR INSULATED FORCEP; 10''(25.5CM), HAND SWITCHING FDA UDI
Model / Reference
B65244 FDA UDI
Description
TEBBETTS ELECTROSURGICAL MONO-POLAR INSULATED FORCEP; 10''(25.5CM), HAND SWITCHING FDA UDI

Identifiers

Catalog Number
B65244 FDA UDI
Primary DI / UDI-DI
B089B652440 FDA UDI
510(k) Number
K072124 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery electrosurgical electrode, monopolar, reusable

Tebbetts Hand-Activated Monopolar Insulated Forcep by Black & Black Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d2b5f4f7-dde9-454f-af2b-31d1ecdc0994 36 fields · synced May 30, 2026