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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
"OFD1-03 Ofodile Series I Silicone Implants" FDA UDI
Model / Reference
OFD1-03 FDA UDI
Description
"OFD1-03 Ofodile Series I Silicone Implants" FDA UDI

Identifiers

Catalog Number
OFD1-03 FDA UDI
Primary DI / UDI-DI
00851988007624 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 bdb1fffe-80cf-4fb7-bc4d-f29cea0a7576 35 fields · synced May 30, 2026