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Medical device manufacturer

Conphar, Inc.

Conphar, Inc. holds 122 FDA 510(k) clearances across 45 product codes. Median elapsed review time is 24 days. openFDA lists no recall records naming the company.

Updated · ingest status · JSON

510(k) clearances
122
Product codes
45
Median review
24 days
Recall records
0

How does FDA spell Conphar, Inc.?

FDA publishes this company under a single spelling, so nothing needed merging here. Many manufacturers are not so tidy.

Which product codes does Conphar, Inc. file in?

45 product codes, ranked by how much they file in each.

Product codes this company holds clearances in, with their median elapsed review time in each.
CodeDeviceClearancesMedian reviewLatest
FZTCutter, Surgical2117 days
GENForceps, General & Plastic Surgery1424 days
DXQBlood Pressure Cuff621 days
KNXCollector, Urine, (And Accessories) For Indwelling Catheter628 days
EGNScissors, Surgical Tissue, Dental525 days
KNTTubes, Gastrointestinal (And Accessories)528 days
KODCatheter, Urological522 days
IQIOrthosis, Limb Brace418 days
EFLForceps, Dressing, Dental324 days
GDFGuide, Needle, Surgical330 days
INPTips And Pads, Cane, Crutch And Walker327 days
LDEStethoscope, Manual319 days
DQDStethoscope, Electronic216 days
DXNSystem, Measurement, Blood-Pressure, Non-Invasive221 days
ERAOtoscope257 days
FQMBandage, Elastic228 days
GDJClamp, Surgical, General & Plastic Surgery28 days
GWZPercussor215 days
HDFSpeculum, Vaginal, Metal220 days
HNFScissors, Ophthalmic224 days
HTDForceps224 days
KGZAccessories, Catheter28 days
BSYCatheters, Suction, Tracheobronchial124 days
BZBCatheter, Nasal, Oxygen118 days
CAEAirway, Oropharyngeal, Anesthesiology16 days

Showing the 25 they file in most, of 45.

Median review is elapsed calendar days between date received and decision date, as published by FDA. It is not FDA review days — the two differ whenever the agency stops the clock for an additional information request.

Source: openFDA device/510k · retrieved

Has Conphar, Inc. had a recall?

openFDA lists no recall records naming this company. That is the absence of a record, not a guarantee — and it counts only recalls FDA has published under a spelling we resolved to this company.

Recall class comes from openFDA's enforcement endpoint, which does not carry every recall — where it is missing, none is shown rather than guessed. Recall class I is the most serious kind of recall; device class I is the least risky kind of device, and the two are never mixed here.

Source: openFDA device/recall · retrieved

What has Conphar, Inc. cleared recently?

Most recent 510(k) clearances for this company, newest first.
510(k)DeviceCodeDecisionElapsed days
K821825CONPHAR SILICONE FEEDING TUBEKNT49
K821354CONPHAR MAYO HEGAR NEEDLE HOLDERGDF29
K821295OLSEN HEGAR NEEDLE HOLDERSGDF30
K821289MAYO-HEGAR NEEDLE HOLDERGDF30
K821298BACKHAUS CLAMP, 3 1/2HTD24
K821294TONSIL SCISSORS STRAIGHT 5 1/2EGN24
K821293BACKHAUS CLAMP, 5 1/4HTD24
K821292TONSIL SCISSORS 7EGN24
K821290LITTAUER SCISSORS 5 1/2HNF24
K821286IRIS SCISSORS STRAIGHT 4 1/2HNF24

Source: openFDA device/510k · retrieved

Watch what Conphar, Inc. files next

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Data on this page comes from FDA's public openFDA API and is US public domain (CC0). DeviceSignal is an independent commercial service and is not affiliated with the U.S. Food and Drug Administration. Information only, not regulatory advice. Verify anything you rely on against open.fda.gov.