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Surgistar

FDA UDI

Class I (US FDA UDI)

by Surgistar Inc.

Identity

Trade Name
SURGISTAR FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Model / Reference
0420 FDA UDI

Identifiers

Primary DI / UDI-DI
00878799000033 FDA UDI
510(k) Number
K923689 FDA UDI
FDA Product Code
GDX FDA UDI
GMDN Term
Manual scalpel blade, single-use 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual scalpel blade, single-use

Surgistar by Surgistar Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgistar Inc.

Sources (1)

  • FDA UDI 10d9a2aa-254e-4320-b60f-db226b4789be 34 fields · synced Jun 1, 2026