← Back to catalogue

Symmetry Hibbs

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Hibbs FDA UDI
Generic Name
Orthopaedic osteotome FDA UDI
Device Name
Symmetry® Osteotome, Hibbs, Straight, 3/4 in (19 mm) Wide, 9 1/2 in, 241 mm FDA UDI
Model / Reference
28-5120 FDA UDI
Description
Symmetry® Osteotome, Hibbs, Straight, 3/4 in (19 mm) Wide, 9 1/2 in, 241 mm FDA UDI

Identifiers

Catalog Number
28-5120 FDA UDI
Primary DI / UDI-DI
00887482065082 FDA UDI
FDA Product Code
HWM FDA UDI
GMDN Term
Orthopaedic osteotome FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 9.5 Inch FDA UDI
Width — 0.75 Inch FDA UDI

Category: Orthopaedic osteotome

Symmetry Hibbs by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic osteotome.

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

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI b28d57d8-0e24-4de2-ac09-5547f441698a 36 fields · synced Jun 1, 2026