← Back to catalogue

Peri-Pyriform™

FDA UDI

Class II (US FDA UDI)

by Implantech Associates, Inc.

Identity

Trade Name
Peri-Pyriform™ FDA UDI
Generic Name
Nasal cartilage support implant, non-bioabsorbable FDA UDI
Device Name
Premaxillary Implant FDA UDI
Model / Reference
Size: Medium FDA UDI
Description
Premaxillary Implant FDA UDI

Identifiers

Catalog Number
BPI-M FDA UDI
Primary DI / UDI-DI
M724BPIM1 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal cartilage support implant, non-bioabsorbable

Peri-Pyriform™ by Implantech Associates, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
Implantech Associates, Inc.

Sources (1)

  • FDA UDI 5f8a5f34-ea41-4d37-aa49-03d3cf561db5 35 fields · synced Jun 9, 2026