FDA Registration
Active
🇺🇸 United States
DPY - P.F.C., PFC ULTIMA HIP SYSTEM TRIAL (85592X), Device Listing: Q019772
Reg #: 3009882462
·
FEI: 3009882462
·
Expires 2025
Products
1
Proprietary Names
39
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- PERRYMAN COMPANY
- Registration Number
- 3009882462
- FEI Number
- 3009882462
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 149 S Johnson Rd
- City
- Houston
- State
- PA
- ZIP
- 15342
- Country
- US
Owner / Operator
- Firm Name
- Perryman Company
- Operator Number
- 10042198
- Address
- 149 South Johnson Rd
- City
- Houston
- State
- PA
- Postal Code
- 15342
- Country
- US
- Correspondent
- Dylan Crawford
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Template | HWT | Class 1 | Orthopedic | No | 2013-01-22 |
Proprietary Names
DPY - P.F.C., PFC ULTIMA HIP SYSTEM TRIAL (85592X), Device Listing: Q019772
DPY - SKYLINE, SIZING TRIALS (410270XXX), Device Listing: D112268
DPY - PINNACLE, PINNACLE TRIAL LINERS, Device Listing: Q019772
DPY - PINNACLE,EN, ALTERNATE BEARING TRIAL LINER (2218891XX), Device Listing: Q019772
DPY - GLOBAL ADVANTAGE, GLOBAL ADVANTAGE HEAD TRIAL (2128650X0), Device Listing: Q019772
DPY - PINNACLE & PINNACLE BANTEM, EN,- BANTAM PINNACLE TRIAL LINERS (221822_28XXX), Device Listing: Q019772
DPY - ATTUNE®, ATTUNE BAL BLK POSITIONER (25450551X) Device Listing: Q019772
ART - Augmented MGS Baseplate Trial, AUGMENT BASEPLATE TRIAL, (AR-9593-2XXX), Device Listing: D223058
DPY - S-ROM, S-ROM FEMORAL HEAD TRIAL (8759XX), Device Listing: (Q019772)
DPY - GLOBAL ANCHOR PEG GLENOID, ANCHOR PEG GLENOID TRIAL (2236800X0), Device Listing: Q019772
DPY - PINNACLE, EN - REVISION PINNACLE TRIAL LINER (221836XXX), Device Listing: Q019772
DPY - SIGMA,EN, PFC SIGMA TC3 RP TIB TRIAL INS ASSEMBLY (9633XX), Device Listing: Q019772
DPY - GLOBAL UNITE, GLOBAL UNITE CELCON GD (210061071), Device Listing: Q019772
DPY - ATTUNE KNEE SYSTEM,EN - ATTUNE, REVISION FB INSERT TRIAL, (25170XXXX). Device Listing: Q019772
FULL AUGMENT SIZERS / FULL AUGMENT TRIALS
ART - iBalance UKA®, Tibial Bearing Trial, UNI-KNEE TIBIAL BEARING (AR-601-TBXX), Device Listing: D223058
GLENOSPHERE TRIAL (38mm & 42mm)
PEG GLENOID TRIAL (SMALL, MEDIUM, LARGE, XLARGE)
EXP HEAD TRIAL (47MM, 50MM, 53MM)
DPY - PINNACLE, PINNACLE MB HEAD TRIALS (22172XXXX), Device Listing: Q019772
PERFORM Humeral System
EXT HEAD TRIAL (XSHORT, SHORT, TALL)
Equinoxe - EXT B047065
ART - iBalance UKA®, Tibial D-Ring Trial, TRIAL BASE PLATE, (AR-611-3X), Device Listing, D223058
Tornier Perform Humeral System
LEGION (LGN STD CR INSERT TRIALS, 8111411X) Device Listing R060915
LEGION (PS INSERT TRIALS, 8111XXXX) Device Listing R060915
DPY - EMPHASYS, EMSYS MB Head Trial (4830XXXXX), Device Listing: Q019772
DPY - DPS TRIAL HEADS (4831XXXXX), Device Listing: Q019772
DPY - SIGMA,EN, PFC SIGMA RP TRIAL (973XXX), Device Listing: Q019772
DPY - ATTUNE®, ATTUNE CR MEDIAL STABILIZED TRIAL (2547XXXXX) Device Listing: Q019772
DPY - PINNACLE, EN - PINNACLE TRIAL LINERS, Device Listing: Q019772
DPY - EMPHASYS, EMSYS DM Trial Liner (4825XXXXX), Device Listing: Q019772
DPY - GLOBAL APG+, APG+ Trial (2236000XX), Device Listing: Q019772
DPY - ATTUNE KNEE SYSTEM,EN - ATTUNE, REVISION RP INSERT TRIAL, (25171XXXX). Device Listing: Q019772
ART - Univers Revers Trial Humeral Insert, TRIAL HUMERAL INSERT, (AR-9530XS-0X(c)) Device Listing: D223058
DPY - P.F.C., DOME PATELLA TRIAL (86613X), Device Listing: Q019772
DPY - PINNACLE, DUAL MOBILITY LINER TRIAL (221848_66XXX), Device Listing: Q019772
DPY - EMPHASYS, EMSYS Trial Liners (4821XXXXX), Device Listing: Q019772
Establishment Types
Manufacture Medical Device for Another Party (Contract Manufacturer)