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Surgiform

FDA UDI

Class II (US FDA UDI)

by Surgical Technology Laboratories Inc.

Identity

Trade Name
SURGIFORM FDA UDI
Generic Name
Nasal cartilage support implant, non-bioabsorbable FDA UDI
Device Name
CDC-09D Nasal Cresent Dorsal Series Columella Silicone Implants FDA UDI
Model / Reference
CDC-09D FDA UDI
Description
CDC-09D Nasal Cresent Dorsal Series Columella Silicone Implants FDA UDI

Identifiers

Catalog Number
CDC-09D FDA UDI
Primary DI / UDI-DI
00850987007758 FDA UDI
510(k) Number
K983755 FDA UDI
FDA Product Code
FZE FDA UDI
GMDN Term
Nasal cartilage support implant, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal cartilage support implant, non-bioabsorbable

Surgiform by Surgical Technology Laboratories Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal cartilage support implant, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eea9e6f8-1a60-4ddc-a72e-ff098ed66f9f 35 fields · synced Jun 8, 2026