510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K832153Substantially Equivalent

Pdm Siloxane Prosthetic Nose

Delaware Prosthetics, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832153 is the FDA 510(k) clearance record for PDM SILOXANE PROSTHETIC NOSE, a class I device, cleared for Delaware Prosthetics, Inc. on under FDA product code GBI (Material, External Aesthetic Restoration, Used With Adhesive). FDA records list 5 510(k) clearances for Delaware Prosthetics, Inc., from to . As of , FDA records show no recalls naming K832153.

Clearance record

Decision date
Received
(157 days to decision)
Product code
GBI Material, External Aesthetic Restoration, Used With Adhesive
Regulation
21 CFR 878.3800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Delaware Prosthetics, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code GBI

Trailing 12 months

FDA records hold no clearances under product code GBI in the trailing twelve months.

FDA records show no clearances under product code GBI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GBI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260