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HNM Medical

FDA UDI

Class I (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name
HNM Medical FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
SPINAL FUSION CURETTE, 9", #00, OVAL, REVERSE ANG DOWN FDA UDI
Model / Reference
HNM-1-29-5514 FDA UDI
Description
SPINAL FUSION CURETTE, 9", #00, OVAL, REVERSE ANG DOWN FDA UDI

Identifiers

Catalog Number
HNM-1-29-5514 FDA UDI
Primary DI / UDI-DI
00842962117682 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Bone curette, reusable 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

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone curette, reusable

HNM Medical's Bone Curette, a versatile and durable manual surgical instrument designed for cutting and excising bone tissue in orthopaedic or plastic surgery procedures. Made from high-grade stainless steel, it is a common choice for bone removal without causing trauma to surrounding muscles. The device features a long, slender handle with a concave tip, facilitating precise cuts while minimizing damage.

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hnm Stainless, Llc.

Sources (1)

  • FDA UDI 94477ebb-d360-486b-9a9c-d7d788620729 34 fields · synced Jul 18, 2026